SNP Links for Nucleotide (Select 635372960) - SNP

Links from Nucleotide

Items: 1 to 20 of 516

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Select item 14909324011.

rs1490932401 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:6900328 (GRCh38)
17:6803647 (GRCh37)
Canonical SPDI:: NC_000017.11:6900327:T:C
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.6900328T>C, NC_000017.10:g.6803647T>C, NR_002710.2:n.2747T>C, NR_120453.1:n.2194T>C

Select item 14877430592.

rs1487743059 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:6900182 (GRCh38)
17:6803501 (GRCh37)
Canonical SPDI:: NC_000017.11:6900181:C:T
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_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_000017.11:g.6900182C>T, NC_000017.10:g.6803501C>T, NR_002710.2:n.2601C>T, NR_120453.1:n.2048C>T

Select item 14864751103.

rs1486475110 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:6896351 (GRCh38)
17:6799670 (GRCh37)
Canonical SPDI:: NC_000017.11:6896350:G:A
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000214/3 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000043/6 (GnomAD)
HGVS:: NC_000017.11:g.6896351G>A, NC_000017.10:g.6799670G>A, NR_002710.2:n.1400G>A, NR_120453.1:n.760G>A

Select item 14850056314.

rs1485005631 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 17:6898206 (GRCh38)
17:6801525 (GRCh37)
Canonical SPDI:: NC_000017.11:6898205:C:G
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.6898206C>G, NC_000017.10:g.6801525C>G, NR_120453.1:n.1081C>G

Select item 14842805185.

rs1484280518 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:6895199 (GRCh38)
17:6798518 (GRCh37)
Canonical SPDI:: NC_000017.11:6895198:G:C
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000017.11:g.6895199G>C, NC_000017.10:g.6798518G>C, NR_002710.2:n.1203G>C, NR_120453.1:n.563G>C

Select item 14838868706.

rs1483886870 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:6898828 (GRCh38)
17:6802147 (GRCh37)
Canonical SPDI:: NC_000017.11:6898827:G:A
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.6898828G>A, NC_000017.10:g.6802147G>A, NR_002710.2:n.1917G>A, NR_120453.1:n.1364G>A

Select item 14835895327.

rs1483589532 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:6894954 (GRCh38)
17:6798273 (GRCh37)
Canonical SPDI:: NC_000017.11:6894953:G:A
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
HGVS:: NC_000017.11:g.6894954G>A, NC_000017.10:g.6798273G>A, NR_002710.2:n.1047G>A, NR_120453.1:n.407G>A

Select item 14803601938.

rs1480360193 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:6896628 (GRCh38)
17:6799947 (GRCh37)
Canonical SPDI:: NC_000017.11:6896627:G:A
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.6896628G>A, NC_000017.10:g.6799947G>A, NR_002710.2:n.1583G>A, NR_120453.1:n.943G>A

Select item 14786538879.

rs1478653887 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCTCCACCAGGCACGTATGCAAAAGACCTTCACAA>- [Show Flanks]
Chromosome:: 17:6899697 (GRCh38)
17:6803016 (GRCh37)
Canonical SPDI:: NC_000017.11:6899693:CAATCTCCACCAGGCACGTATGCAAAAGACCTTCACAA:CAA
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.6899697_6899731del, NC_000017.10:g.6803016_6803050del, NR_002710.2:n.2223_2257del, NR_120453.1:n.1670_1704del

Select item 147819186910.

rs1478191869 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:6895347 (GRCh38)
17:6798666 (GRCh37)
Canonical SPDI:: NC_000017.11:6895346:G:A
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.6895347G>A, NC_000017.10:g.6798666G>A, NR_002710.2:n.1208G>A, NR_120453.1:n.568G>A

Select item 147710978311.

rs1477109783 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:6896437 (GRCh38)
17:6799756 (GRCh37)
Canonical SPDI:: NC_000017.11:6896436:G:C
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.6896437G>C, NC_000017.10:g.6799756G>C, NR_002710.2:n.1486G>C, NR_120453.1:n.846G>C

Select item 147679794612.

rs1476797946 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 17:6894986 (GRCh38)
17:6798305 (GRCh37)
Canonical SPDI:: NC_000017.11:6894985:T:C,NC_000017.11:6894985:T:G
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
C=0.000035/1 (TOMMO)
HGVS:: NC_000017.11:g.6894986T>C, NC_000017.11:g.6894986T>G, NC_000017.10:g.6798305T>C, NC_000017.10:g.6798305T>G, NR_002710.2:n.1079T>C, NR_002710.2:n.1079T>G, NR_120453.1:n.439T>C, NR_120453.1:n.439T>G

Select item 147439772913.

rs1474397729 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 17:6900263 (GRCh38)
17:6803582 (GRCh37)
Canonical SPDI:: NC_000017.11:6900262:C:A
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.6900263C>A, NC_000017.10:g.6803582C>A, NR_002710.2:n.2682C>A, NR_120453.1:n.2129C>A

Select item 147387947314.

rs1473879473 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:6900302 (GRCh38)
17:6803621 (GRCh37)
Canonical SPDI:: NC_000017.11:6900301:A:C
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000038/10 (TOPMED)
C=0.000057/8 (GnomAD)
HGVS:: NC_000017.11:g.6900302A>C, NC_000017.10:g.6803621A>C, NR_002710.2:n.2721A>C, NR_120453.1:n.2168A>C

Select item 147164472415.

rs1471644724 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:6893797 (GRCh38)
17:6797116 (GRCh37)
Canonical SPDI:: NC_000017.11:6893796:G:A
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.6893797G>A, NC_000017.10:g.6797116G>A, NR_120453.1:n.21G>A, XR_007065597.1:n.842C>T

Select item 147151629416.

rs1471516294 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 17:6899870 (GRCh38)
17:6803189 (GRCh37)
Canonical SPDI:: NC_000017.11:6899869:T:C,NC_000017.11:6899869:T:G
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000017.11:g.6899870T>C, NC_000017.11:g.6899870T>G, NC_000017.10:g.6803189T>C, NC_000017.10:g.6803189T>G, NR_002710.2:n.2289T>C, NR_002710.2:n.2289T>G, NR_120453.1:n.1736T>C, NR_120453.1:n.1736T>G

Select item 147049447917.

rs1470494479 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:6893878 (GRCh38)
17:6797197 (GRCh37)
Canonical SPDI:: NC_000017.11:6893877:G:A,NC_000017.11:6893877:G:T
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.6893878G>A, NC_000017.11:g.6893878G>T, NC_000017.10:g.6797197G>A, NC_000017.10:g.6797197G>T, NR_120453.1:n.102G>A, NR_120453.1:n.102G>T, XR_007065597.1:n.761C>T, XR_007065597.1:n.761C>A

Select item 146953039718.

rs1469530397 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:6893788 (GRCh38)
17:6797107 (GRCh37)
Canonical SPDI:: NC_000017.11:6893787:A:G
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000017.11:g.6893788A>G, NC_000017.10:g.6797107A>G, NR_120453.1:n.12A>G, XR_007065597.1:n.851T>C

Select item 146361225019.

rs1463612250 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 17:6896582 (GRCh38)
17:6799901 (GRCh37)
Canonical SPDI:: NC_000017.11:6896581:C:G
Gene:: ALOX12P2 (Varview), LOC124903908 (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000017.11:g.6896582C>G, NC_000017.10:g.6799901C>G, NR_002710.2:n.1537C>G, NR_120453.1:n.897C>G

Select item 146356833720.

rs1463568337 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:6899420 (GRCh38)
17:6802739 (GRCh37)
Canonical SPDI:: NC_000017.11:6899419:A:G
Gene:: ALOX12P2 (Varview)
Functional Consequence:: non_coding_transcript_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_000017.11:g.6899420A>G, NC_000017.10:g.6802739A>G, NR_002710.2:n.2048A>G, NR_120453.1:n.1495A>G

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