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Select item 14914494841.

rs1491449484 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 1:162022245 (GRCh38)
1:161992036 (GRCh37)
Canonical SPDI:: NC_000001.11:162022245:T:TCT
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000001.11:g.162022246_162022247insCT, NC_000001.10:g.161992036_161992037insCT, NG_052853.1:g.7220_7221insGA

Select item 14913482902.

rs1491348290 has merged into rs56395023 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,TT,TTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:162022253 (GRCh38)
1:161992043 (GRCh37)
Canonical SPDI:: NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:162022244:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
-=0.0794/306 (ALSPAC)
HGVS:: NC_000001.11:g.162022253_162022268del, NC_000001.11:g.162022255_162022268del, NC_000001.11:g.162022256_162022268del, NC_000001.11:g.162022258_162022268del, NC_000001.11:g.162022259_162022268del, NC_000001.11:g.162022261_162022268del, NC_000001.11:g.162022262_162022268del, NC_000001.11:g.162022263_162022268del, NC_000001.11:g.162022264_162022268del, NC_000001.11:g.162022265_162022268del, NC_000001.11:g.162022266_162022268del, NC_000001.11:g.162022267_162022268del, NC_000001.11:g.162022268del, NC_000001.11:g.162022268dup, NC_000001.11:g.162022267_162022268dup, NC_000001.11:g.162022266_162022268dup, NC_000001.11:g.162022265_162022268dup, NC_000001.11:g.162022264_162022268dup, NC_000001.11:g.162022263_162022268dup, NC_000001.11:g.162022262_162022268dup, NC_000001.11:g.162022261_162022268dup, NC_000001.11:g.162022260_162022268dup, NC_000001.11:g.162022259_162022268dup, NC_000001.11:g.162022258_162022268dup, NC_000001.11:g.162022257_162022268dup, NC_000001.11:g.162022256_162022268dup, NC_000001.11:g.162022255_162022268dup, NC_000001.11:g.162022254_162022268dup, NC_000001.11:g.162022253_162022268dup, NC_000001.11:g.162022252_162022268dup, NC_000001.11:g.162022251_162022268dup, NC_000001.11:g.162022250_162022268dup, NC_000001.11:g.162022249_162022268dup, NC_000001.11:g.162022248_162022268dup, NC_000001.11:g.162022247_162022268dup, NC_000001.11:g.162022246_162022268dup, NC_000001.11:g.162022245_162022268dup, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.162022268_162022269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992043_161992058del, NC_000001.10:g.161992045_161992058del, NC_000001.10:g.161992046_161992058del, NC_000001.10:g.161992048_161992058del, NC_000001.10:g.161992049_161992058del, NC_000001.10:g.161992051_161992058del, NC_000001.10:g.161992052_161992058del, NC_000001.10:g.161992053_161992058del, NC_000001.10:g.161992054_161992058del, NC_000001.10:g.161992055_161992058del, NC_000001.10:g.161992056_161992058del, NC_000001.10:g.161992057_161992058del, NC_000001.10:g.161992058del, NC_000001.10:g.161992058dup, NC_000001.10:g.161992057_161992058dup, NC_000001.10:g.161992056_161992058dup, NC_000001.10:g.161992055_161992058dup, NC_000001.10:g.161992054_161992058dup, NC_000001.10:g.161992053_161992058dup, NC_000001.10:g.161992052_161992058dup, NC_000001.10:g.161992051_161992058dup, NC_000001.10:g.161992050_161992058dup, NC_000001.10:g.161992049_161992058dup, NC_000001.10:g.161992048_161992058dup, NC_000001.10:g.161992047_161992058dup, NC_000001.10:g.161992046_161992058dup, NC_000001.10:g.161992045_161992058dup, NC_000001.10:g.161992044_161992058dup, NC_000001.10:g.161992043_161992058dup, NC_000001.10:g.161992042_161992058dup, NC_000001.10:g.161992041_161992058dup, NC_000001.10:g.161992040_161992058dup, NC_000001.10:g.161992039_161992058dup, NC_000001.10:g.161992038_161992058dup, NC_000001.10:g.161992037_161992058dup, NC_000001.10:g.161992036_161992058dup, NC_000001.10:g.161992035_161992058dup, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.161992058_161992059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052853.1:g.7206_7221del, NG_052853.1:g.7208_7221del, NG_052853.1:g.7209_7221del, NG_052853.1:g.7211_7221del, NG_052853.1:g.7212_7221del, NG_052853.1:g.7214_7221del, NG_052853.1:g.7215_7221del, NG_052853.1:g.7216_7221del, NG_052853.1:g.7217_7221del, NG_052853.1:g.7218_7221del, NG_052853.1:g.7219_7221del, NG_052853.1:g.7220_7221del, NG_052853.1:g.7221del, NG_052853.1:g.7221dup, NG_052853.1:g.7220_7221dup, NG_052853.1:g.7219_7221dup, NG_052853.1:g.7218_7221dup, NG_052853.1:g.7217_7221dup, NG_052853.1:g.7216_7221dup, NG_052853.1:g.7215_7221dup, NG_052853.1:g.7214_7221dup, NG_052853.1:g.7213_7221dup, NG_052853.1:g.7212_7221dup, NG_052853.1:g.7211_7221dup, NG_052853.1:g.7210_7221dup, NG_052853.1:g.7209_7221dup, NG_052853.1:g.7208_7221dup, NG_052853.1:g.7207_7221dup, NG_052853.1:g.7206_7221dup, NG_052853.1:g.7205_7221dup, NG_052853.1:g.7204_7221dup, NG_052853.1:g.7203_7221dup, NG_052853.1:g.7202_7221dup, NG_052853.1:g.7201_7221dup, NG_052853.1:g.7200_7221dup, NG_052853.1:g.7199_7221dup, NG_052853.1:g.7198_7221dup, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052853.1:g.7221_7222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14913293373.

rs1491329337 has merged into rs60065337 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA [Show Flanks]
Chromosome:: 1:162025599 (GRCh38)
1:161995389 (GRCh37)
Canonical SPDI:: NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:162025586:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA
Gene:: OLFML2B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.1661/640 (ALSPAC)
A=0.1721/862 (1000Genomes)
HGVS:: NC_000001.11:g.162025599_162025602del, NC_000001.11:g.162025600_162025602del, NC_000001.11:g.162025601_162025602del, NC_000001.11:g.162025602del, NC_000001.11:g.162025602dup, NC_000001.11:g.162025601_162025602dup, NC_000001.11:g.162025600_162025602dup, NC_000001.11:g.162025599_162025602dup, NC_000001.11:g.162025598_162025602dup, NC_000001.10:g.161995389_161995392del, NC_000001.10:g.161995390_161995392del, NC_000001.10:g.161995391_161995392del, NC_000001.10:g.161995392del, NC_000001.10:g.161995392dup, NC_000001.10:g.161995391_161995392dup, NC_000001.10:g.161995390_161995392dup, NC_000001.10:g.161995389_161995392dup, NC_000001.10:g.161995388_161995392dup, NG_052853.1:g.3876_3879del, NG_052853.1:g.3877_3879del, NG_052853.1:g.3878_3879del, NG_052853.1:g.3879del, NG_052853.1:g.3879dup, NG_052853.1:g.3878_3879dup, NG_052853.1:g.3877_3879dup, NG_052853.1:g.3876_3879dup, NG_052853.1:g.3875_3879dup

Select item 14911538354.

rs1491153835 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CAGAGAGAGA [Show Flanks]
Chromosome:: 1:161993077 (GRCh38)
1:161962868 (GRCh37)
Canonical SPDI:: NC_000001.11:161993077:AGAGAGAGACAGAGAGAGA:AGAGAGAGACAGAGAGAGACAGAGAGAGA
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAGACAGAGAGAGACAGAGAGAGA=0.0002/1 (ALFA)
AGAGAGAGAC=0.0002/1 (Estonian)
HGVS:: NC_000001.11:g.161993087_161993096dup, NC_000001.10:g.161962877_161962886dup, NG_052853.1:g.36379_36388dup

Select item 14908854705.

rs1490885470 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:161983943 (GRCh38)
1:161953733 (GRCh37)
Canonical SPDI:: NC_000001.11:161983942:G:A,NC_000001.11:161983942:G:T
Gene:: OLFML2B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000177/3 (TOMMO)
T=0.000342/1 (KOREAN)
T=0.000546/1 (Korea1K)
HGVS:: NC_000001.11:g.161983943G>A, NC_000001.11:g.161983943G>T, NC_000001.10:g.161953733G>A, NC_000001.10:g.161953733G>T, NG_052853.1:g.45523C>T, NG_052853.1:g.45523C>A, NM_015441.2:c.1985C>T, NM_015441.2:c.1985C>A, NM_015441.3:c.1985C>T, NM_015441.3:c.1985C>A, NM_015441.1:c.1985C>T, NM_015441.1:c.1985C>A, NM_001347700.1:c.1991C>T, NM_001347700.1:c.1991C>A, NM_001347700.2:c.1991C>T, NM_001347700.2:c.1991C>A, NM_001297713.1:c.1988C>T, NM_001297713.1:c.1988C>A, NM_001297713.2:c.1988C>T, NM_001297713.2:c.1988C>A, XM_011509398.3:c.1265C>T, XM_011509398.3:c.1265C>A, XM_011509398.2:c.1265C>T, XM_011509398.2:c.1265C>A, XM_011509398.1:c.1265C>T, XM_011509398.1:c.1265C>A, NP_056256.1:p.Thr662Ile, NP_056256.1:p.Thr662Asn, NP_001334629.1:p.Thr664Ile, NP_001334629.1:p.Thr664Asn, NP_001284642.1:p.Thr663Ile, NP_001284642.1:p.Thr663Asn, XP_011507700.1:p.Thr422Ile, XP_011507700.1:p.Thr422Asn

Select item 14908220636.

rs1490822063 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:161985981 (GRCh38)
1:161955771 (GRCh37)
Canonical SPDI:: NC_000001.11:161985980:T:C
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.161985981T>C, NC_000001.10:g.161955771T>C, NG_052853.1:g.43485A>G

Select item 14908045517.

rs1490804551 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:162001734 (GRCh38)
1:161971524 (GRCh37)
Canonical SPDI:: NC_000001.11:162001733:T:C
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.162001734T>C, NC_000001.10:g.161971524T>C, NG_052853.1:g.27732A>G

Select item 14907142858.

rs1490714285 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 1:162023126 (GRCh38)
1:161992916 (GRCh37)
Canonical SPDI:: NC_000001.11:162023125:A:G,NC_000001.11:162023125:A:T
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000248/4 (TOMMO)
T=0.000546/1 (Korea1K)
T=0.001027/3 (KOREAN)
HGVS:: NC_000001.11:g.162023126A>G, NC_000001.11:g.162023126A>T, NC_000001.10:g.161992916A>G, NC_000001.10:g.161992916A>T, NG_052853.1:g.6340T>C, NG_052853.1:g.6340T>A

Select item 14906139679.

rs1490613967 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:162018184 (GRCh38)
1:161987974 (GRCh37)
Canonical SPDI:: NC_000001.11:162018183:T:G
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.162018184T>G, NC_000001.10:g.161987974T>G, NG_052853.1:g.11282A>C

Select item 149037818210.

rs1490378182 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 1:161994284 (GRCh38)
1:161964074 (GRCh37)
Canonical SPDI:: NC_000001.11:161994283:A:C,NC_000001.11:161994283:A:T
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
C=0.003821/7 (Korea1K)
HGVS:: NC_000001.11:g.161994284A>C, NC_000001.11:g.161994284A>T, NC_000001.10:g.161964074A>C, NC_000001.10:g.161964074A>T, NG_052853.1:g.35182T>G, NG_052853.1:g.35182T>A

Select item 149034590711.

rs1490345907 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:162011186 (GRCh38)
1:161980976 (GRCh37)
Canonical SPDI:: NC_000001.11:162011185:C:T
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.162011186C>T, NC_000001.10:g.161980976C>T, NG_052853.1:g.18280G>A

Select item 149032227712.

rs1490322277 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:162026348 (GRCh38)
1:161996138 (GRCh37)
Canonical SPDI:: NC_000001.11:162026347:G:A,NC_000001.11:162026347:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00003/8 (TOPMED)
C=0.000043/6 (GnomAD)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.162026348G>A, NC_000001.11:g.162026348G>C, NC_000001.10:g.161996138G>A, NC_000001.10:g.161996138G>C, NG_052853.1:g.3118C>T, NG_052853.1:g.3118C>G

Select item 149028861113.

rs1490288611 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:162020458 (GRCh38)
1:161990248 (GRCh37)
Canonical SPDI:: NC_000001.11:162020457:C:T
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.00003/8 (TOPMED)
T=0.000036/5 (GnomAD)
HGVS:: NC_000001.11:g.162020458C>T, NC_000001.10:g.161990248C>T, NG_052853.1:g.9008G>A

Select item 148998061414.

rs1489980614 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:161987678 (GRCh38)
1:161957468 (GRCh37)
Canonical SPDI:: NC_000001.11:161987677:C:G,NC_000001.11:161987677:C:T
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.00011/2 (TOMMO)
HGVS:: NC_000001.11:g.161987678C>G, NC_000001.11:g.161987678C>T, NC_000001.10:g.161957468C>G, NC_000001.10:g.161957468C>T, NG_052853.1:g.41788G>C, NG_052853.1:g.41788G>A

Select item 148995667815.

rs1489956678 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:162003226 (GRCh38)
1:161973016 (GRCh37)
Canonical SPDI:: NC_000001.11:162003225:A:G
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.162003226A>G, NC_000001.10:g.161973016A>G, NG_052853.1:g.26240T>C

Select item 148990997416.

rs1489909974 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:162004258 (GRCh38)
1:161974048 (GRCh37)
Canonical SPDI:: NC_000001.11:162004257:C:T
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.162004258C>T, NC_000001.10:g.161974048C>T, NG_052853.1:g.25208G>A, XM_011509398.3:c.-500G>A, XM_011509398.2:c.-500G>A, XM_011509398.1:c.-500G>A

Select item 148951441617.

rs1489514416 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:162023876 (GRCh38)
1:161993666 (GRCh37)
Canonical SPDI:: NC_000001.11:162023875:C:T
Gene:: OLFML2B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000001.11:g.162023876C>T, NC_000001.10:g.161993666C>T, NG_052853.1:g.5590G>A, NM_015441.2:c.-446G>A, NM_001347700.1:c.-446G>A, NM_001297713.1:c.-446G>A

Select item 148946572018.

rs1489465720 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:162015912 (GRCh38)
1:161985702 (GRCh37)
Canonical SPDI:: NC_000001.11:162015911:T:A
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.162015912T>A, NC_000001.10:g.161985702T>A, NG_052853.1:g.13554A>T

Select item 148914135019.

rs1489141350 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 1:162023619 (GRCh38)
1:161993409 (GRCh37)
Canonical SPDI:: NC_000001.11:162023618:G:
Gene:: OLFML2B (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000356/5 (ALFA)
-=0.000468/124 (TOPMED)
-=0.000468/3 (1000Genomes)
-=0.000499/70 (GnomAD)
HGVS:: NC_000001.11:g.162023619del, NC_000001.10:g.161993409del, NG_052853.1:g.5847del, NM_015441.2:c.-189del, NM_015441.3:c.-189del, NM_015441.1:c.-189del, NM_001347700.1:c.-189del, NM_001347700.2:c.-189del, NM_001297713.1:c.-189del, NM_001297713.2:c.-189del

Select item 148914000320.

rs1489140003 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:161992367 (GRCh38)
1:161962157 (GRCh37)
Canonical SPDI:: NC_000001.11:161992366:A:T
Gene:: OLFML2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.161992367A>T, NC_000001.10:g.161962157A>T, NG_052853.1:g.37099T>A

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