SNP Links for Gene (Select 219445) - SNP

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Select item 14914960391.

rs1491496039 has merged into rs35577319 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 11:55980444 (GRCh38)
11:55747920 (GRCh37)
Canonical SPDI:: NC_000011.10:55980436:AAAAAAAAA:AAAAAAA,NC_000011.10:55980436:AAAAAAAAA:AAAAAAAA,NC_000011.10:55980436:AAAAAAAAA:AAAAAAAAAA,NC_000011.10:55980436:AAAAAAAAA:AAAAAAAAAAA
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.16157/296 (Korea1K)
-=0.19124/3205 (TOMMO)
-=0.24735/1191 (1000Genomes)
HGVS:: NC_000011.10:g.55980444_55980445del, NC_000011.10:g.55980445del, NC_000011.10:g.55980445dup, NC_000011.10:g.55980444_55980445dup, NC_000011.9:g.55747920_55747921del, NC_000011.9:g.55747921del, NC_000011.9:g.55747921dup, NC_000011.9:g.55747920_55747921dup

Select item 14911070252.

rs1491107025 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: 11:55987029 (GRCh38)
11:55754505 (GRCh37)
Canonical SPDI:: NC_000011.10:55987027:GTG:G
Gene:: OR7E5P (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000011.10:g.55987029_55987030del, NC_000011.9:g.55754505_55754506del

Select item 14910831633.

rs1491083163 has merged into rs35577319 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 11:55980444 (GRCh38)
11:55747920 (GRCh37)
Canonical SPDI:: NC_000011.10:55980436:AAAAAAAAA:AAAAAAA,NC_000011.10:55980436:AAAAAAAAA:AAAAAAAA,NC_000011.10:55980436:AAAAAAAAA:AAAAAAAAAA,NC_000011.10:55980436:AAAAAAAAA:AAAAAAAAAAA
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.16157/296 (Korea1K)
-=0.19124/3205 (TOMMO)
-=0.24735/1191 (1000Genomes)
HGVS:: NC_000011.10:g.55980444_55980445del, NC_000011.10:g.55980445del, NC_000011.10:g.55980445dup, NC_000011.10:g.55980444_55980445dup, NC_000011.9:g.55747920_55747921del, NC_000011.9:g.55747921del, NC_000011.9:g.55747921dup, NC_000011.9:g.55747920_55747921dup

Select item 14907812324.

rs1490781232 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:55980782 (GRCh38)
11:55748258 (GRCh37)
Canonical SPDI:: NC_000011.10:55980781:G:A
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.55980782G>A, NC_000011.9:g.55748258G>A

Select item 14904323105.

rs1490432310 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:55987711 (GRCh38)
11:55755187 (GRCh37)
Canonical SPDI:: NC_000011.10:55987710:G:A
Gene:: OR7E5P (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.55987711G>A, NC_000011.9:g.55755187G>A

Select item 14902943826.

rs1490294382 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55983654 (GRCh38)
11:55751130 (GRCh37)
Canonical SPDI:: NC_000011.10:55983653:A:G
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.55983654A>G, NC_000011.9:g.55751130A>G

Select item 14899644977.

rs1489964497 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:55980352 (GRCh38)
11:55747828 (GRCh37)
Canonical SPDI:: NC_000011.10:55980351:T:C
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000043/6 (GnomAD)
C=0.000057/15 (TOPMED)
HGVS:: NC_000011.10:g.55980352T>C, NC_000011.9:g.55747828T>C

Select item 14898349428.

rs1489834942 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 14897283329.

rs1489728332 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:55986883 (GRCh38)
11:55754359 (GRCh37)
Canonical SPDI:: NC_000011.10:55986882:T:A,NC_000011.10:55986882:T:C
Gene:: OR7E5P (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
A=0.000015/2 (GnomAD)
HGVS:: NC_000011.10:g.55986883T>A, NC_000011.10:g.55986883T>C, NC_000011.9:g.55754359T>A, NC_000011.9:g.55754359T>C

Select item 148962610210.

rs1489626102 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55986370 (GRCh38)
11:55753846 (GRCh37)
Canonical SPDI:: NC_000011.10:55986369:C:T
Gene:: OR7E5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.55986370C>T, NC_000011.9:g.55753846C>T, NR_027688.2:n.36G>A, NM_153024.1:c.-520G>A

Select item 148916765511.

rs1489167655 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:55982531 (GRCh38)
11:55750007 (GRCh37)
Canonical SPDI:: NC_000011.10:55982530:A:C
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_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_000011.10:g.55982531A>C, NC_000011.9:g.55750007A>C

Select item 148908748612.

rs1489087486 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 11:55983738 (GRCh38)
11:55751214 (GRCh37)
Canonical SPDI:: NC_000011.10:55983737:A:C,NC_000011.10:55983737:A:G,NC_000011.10:55983737:A:T
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.55983738A>C, NC_000011.10:g.55983738A>G, NC_000011.10:g.55983738A>T, NC_000011.9:g.55751214A>C, NC_000011.9:g.55751214A>G, NC_000011.9:g.55751214A>T

Select item 148885105213.

rs1488851052 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:55985805 (GRCh38)
11:55753281 (GRCh37)
Canonical SPDI:: NC_000011.10:55985804:C:G,NC_000011.10:55985804:C:T
Gene:: OR7E5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000684/2 (KOREAN)
HGVS:: NC_000011.10:g.55985805C>G, NC_000011.10:g.55985805C>T, NC_000011.9:g.55753281C>G, NC_000011.9:g.55753281C>T, NR_027688.2:n.252G>C, NR_027688.2:n.252G>A, NM_153024.1:c.-304G>C, NM_153024.1:c.-304G>A

Select item 148845692814.

rs1488456928 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:55985153 (GRCh38)
11:55752629 (GRCh37)
Canonical SPDI:: NC_000011.10:55985152:G:A
Gene:: OR7E5P (Varview)
Functional Consequence:: 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_000011.10:g.55985153G>A, NC_000011.9:g.55752629G>A

Select item 148840550615.

rs1488405506 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:55984289 (GRCh38)
11:55751765 (GRCh37)
Canonical SPDI:: NC_000011.10:55984288:A:C
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.55984289A>C, NC_000011.9:g.55751765A>C

Select item 148820004316.

rs1488200043 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55986976 (GRCh38)
11:55754452 (GRCh37)
Canonical SPDI:: NC_000011.10:55986975:C:T
Gene:: OR7E5P (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000214/3 (ALFA)
T=0.000035/1 (TOMMO)
T=0.000081/11 (GnomAD)
HGVS:: NC_000011.10:g.55986976C>T, NC_000011.9:g.55754452C>T

Select item 148807793517.

rs1488077935 has merged into rs34540490 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:55978394 (GRCh38)
11:55745870 (GRCh37)
Canonical SPDI:: NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:55978381:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: OR7E5P (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.075/3 (GENOME_DK)
-=0.2656/1330 (1000Genomes)
HGVS:: NC_000011.10:g.55978394_55978424del, NC_000011.10:g.55978395_55978424del, NC_000011.10:g.55978396_55978424del, NC_000011.10:g.55978397_55978424del, NC_000011.10:g.55978398_55978424del, NC_000011.10:g.55978399_55978424del, NC_000011.10:g.55978400_55978424del, NC_000011.10:g.55978401_55978424del, NC_000011.10:g.55978402_55978424del, NC_000011.10:g.55978403_55978424del, NC_000011.10:g.55978404_55978424del, NC_000011.10:g.55978405_55978424del, NC_000011.10:g.55978406_55978424del, NC_000011.10:g.55978407_55978424del, NC_000011.10:g.55978408_55978424del, NC_000011.10:g.55978409_55978424del, NC_000011.10:g.55978410_55978424del, NC_000011.10:g.55978411_55978424del, NC_000011.10:g.55978412_55978424del, NC_000011.10:g.55978413_55978424del, NC_000011.10:g.55978414_55978424del, NC_000011.10:g.55978415_55978424del, NC_000011.10:g.55978416_55978424del, NC_000011.10:g.55978417_55978424del, NC_000011.10:g.55978418_55978424del, NC_000011.10:g.55978419_55978424del, NC_000011.10:g.55978420_55978424del, NC_000011.10:g.55978421_55978424del, NC_000011.10:g.55978422_55978424del, NC_000011.10:g.55978423_55978424del, NC_000011.10:g.55978424del, NC_000011.10:g.55978424dup, NC_000011.10:g.55978423_55978424dup, NC_000011.10:g.55978422_55978424dup, NC_000011.10:g.55978421_55978424dup, NC_000011.10:g.55978420_55978424dup, NC_000011.10:g.55978416_55978424dup, NC_000011.10:g.55978415_55978424dup, NC_000011.10:g.55978414_55978424dup, NC_000011.10:g.55978413_55978424dup, NC_000011.10:g.55978412_55978424dup, NC_000011.10:g.55978411_55978424dup, NC_000011.10:g.55978410_55978424dup, NC_000011.10:g.55978409_55978424dup, NC_000011.10:g.55978407_55978424dup, NC_000011.9:g.55745870_55745900del, NC_000011.9:g.55745871_55745900del, NC_000011.9:g.55745872_55745900del, NC_000011.9:g.55745873_55745900del, NC_000011.9:g.55745874_55745900del, NC_000011.9:g.55745875_55745900del, NC_000011.9:g.55745876_55745900del, NC_000011.9:g.55745877_55745900del, NC_000011.9:g.55745878_55745900del, NC_000011.9:g.55745879_55745900del, NC_000011.9:g.55745880_55745900del, NC_000011.9:g.55745881_55745900del, NC_000011.9:g.55745882_55745900del, NC_000011.9:g.55745883_55745900del, NC_000011.9:g.55745884_55745900del, NC_000011.9:g.55745885_55745900del, NC_000011.9:g.55745886_55745900del, NC_000011.9:g.55745887_55745900del, NC_000011.9:g.55745888_55745900del, NC_000011.9:g.55745889_55745900del, NC_000011.9:g.55745890_55745900del, NC_000011.9:g.55745891_55745900del, NC_000011.9:g.55745892_55745900del, NC_000011.9:g.55745893_55745900del, NC_000011.9:g.55745894_55745900del, NC_000011.9:g.55745895_55745900del, NC_000011.9:g.55745896_55745900del, NC_000011.9:g.55745897_55745900del, NC_000011.9:g.55745898_55745900del, NC_000011.9:g.55745899_55745900del, NC_000011.9:g.55745900del, NC_000011.9:g.55745900dup, NC_000011.9:g.55745899_55745900dup, NC_000011.9:g.55745898_55745900dup, NC_000011.9:g.55745897_55745900dup, NC_000011.9:g.55745896_55745900dup, NC_000011.9:g.55745892_55745900dup, NC_000011.9:g.55745891_55745900dup, NC_000011.9:g.55745890_55745900dup, NC_000011.9:g.55745889_55745900dup, NC_000011.9:g.55745888_55745900dup, NC_000011.9:g.55745887_55745900dup, NC_000011.9:g.55745886_55745900dup, NC_000011.9:g.55745885_55745900dup, NC_000011.9:g.55745883_55745900dup

Select item 148806917618.

rs1488069176 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55987761 (GRCh38)
11:55755237 (GRCh37)
Canonical SPDI:: NC_000011.10:55987760:A:G
Gene:: OR7E5P (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_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_000011.10:g.55987761A>G, NC_000011.9:g.55755237A>G

Select item 148782505419.

rs1487825054 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 11:55981005 (GRCh38)
11:55748481 (GRCh37)
Canonical SPDI:: NC_000011.10:55981004:TT:T
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0.000071/1 (ALFA)
-=0.000019/5 (TOPMED)
-=0.000057/8 (GnomAD)
HGVS:: NC_000011.10:g.55981006del, NC_000011.9:g.55748482del

Select item 148777713920.

rs1487777139 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:55981266 (GRCh38)
11:55748742 (GRCh37)
Canonical SPDI:: NC_000011.10:55981265:T:C
Gene:: OR7E5P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000142/2 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.55981266T>C, NC_000011.9:g.55748742T>C

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