SNP Links for Nucleotide (Select 214830387) - SNP

Links from Nucleotide

Items: 1 to 20 of 243

<< First< Prev

Page of 13

Next >Last >>

Select item 14895895941.

rs1489589594 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:31471482 (GRCh38)
6:31439259 (GRCh37)
Canonical SPDI:: NC_000006.12:31471481:G:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00059/7 (ALFA)
T=0.001436/190 (GnomAD)
T=0.016864/108 (1000Genomes)
T=0.021351/603 (TOMMO)
HGVS:: NC_000006.12:g.31471482G>T, NC_000006.11:g.31439259G>T, NT_113891.3:g.2948807G>T, NT_113891.2:g.2948913G>T, NT_167248.2:g.2727369G>T, NT_167248.1:g.2732965G>T, NT_167245.2:g.2719008G>T, NT_167245.1:g.2724593G>T, NT_167249.2:g.2770727G>T, NT_167249.1:g.2770025G>T, NT_167247.2:g.2813454G>T, NT_167247.1:g.2819039G>T, NR_002812.3:n.254G>T

Select item 14880336632.

rs1488033663 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:31471766 (GRCh38)
6:31439543 (GRCh37)
Canonical SPDI:: NC_000006.12:31471765:G:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.31471766G>T, NC_000006.11:g.31439543G>T, NT_113891.3:g.2949091G>T, NT_113891.2:g.2949197G>T, NT_167248.2:g.2727653G>T, NT_167248.1:g.2733249G>T, NT_167245.2:g.2719292G>T, NT_167245.1:g.2724877G>T, NT_167249.2:g.2771011G>T, NT_167249.1:g.2770309G>T, NT_167247.2:g.2813738G>T, NT_167247.1:g.2819323G>T, NR_002812.3:n.538G>T

Select item 14876229433.

rs1487622943 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31471597 (GRCh38)
6:31439374 (GRCh37)
Canonical SPDI:: NC_000006.12:31471596:C:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.31471597C>T, NC_000006.11:g.31439374C>T, NT_113891.3:g.2948922C>T, NT_113891.2:g.2949028C>T, NT_167248.2:g.2727484C>T, NT_167248.1:g.2733080C>T, NT_167245.2:g.2719123C>T, NT_167245.1:g.2724708C>T, NT_167249.2:g.2770842C>T, NT_167249.1:g.2770140C>T, NT_167247.2:g.2813569C>T, NT_167247.1:g.2819154C>T, NR_002812.3:n.369C>T

Select item 14838261544.

rs1483826154 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 6:31471244 (GRCh38)
6:31439021 (GRCh37)
Canonical SPDI:: NC_000006.12:31471243:T:A,NC_000006.12:31471243:T:G
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00045/2 (ALFA)
A=0.00043/12 (TOMMO)
G=0.00045/2 (Estonian)
HGVS:: NC_000006.12:g.31471244T>A, NC_000006.12:g.31471244T>G, NC_000006.11:g.31439021T>A, NC_000006.11:g.31439021T>G, NT_113891.3:g.2948569T>A, NT_113891.3:g.2948569T>G, NT_113891.2:g.2948675T>A, NT_113891.2:g.2948675T>G, NT_167248.2:g.2727131T>A, NT_167248.2:g.2727131T>G, NT_167248.1:g.2732727T>A, NT_167248.1:g.2732727T>G, NT_167245.2:g.2718770T>A, NT_167245.2:g.2718770T>G, NT_167245.1:g.2724355T>A, NT_167245.1:g.2724355T>G, NT_167249.2:g.2770489T>A, NT_167249.2:g.2770489T>G, NT_167249.1:g.2769787T>A, NT_167249.1:g.2769787T>G, NT_167247.2:g.2813216T>A, NT_167247.2:g.2813216T>G, NT_167247.1:g.2818801T>A, NT_167247.1:g.2818801T>G, NR_002812.3:n.16T>A, NR_002812.3:n.16T>G

Select item 14834993165.

rs1483499316 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:31472399 (GRCh38)
6:31440176 (GRCh37)
Canonical SPDI:: NC_000006.12:31472398:G:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000006.12:g.31472399G>T, NC_000006.11:g.31440176G>T, NT_113891.3:g.2949724G>T, NT_113891.2:g.2949830G>T, NT_167248.2:g.2728286G>T, NT_167248.1:g.2733882G>T, NT_167245.2:g.2719925G>T, NT_167245.1:g.2725510G>T, NT_167249.2:g.2771644G>T, NT_167249.1:g.2770942G>T, NT_167247.2:g.2814371G>T, NT_167247.1:g.2819956G>T, NR_002812.3:n.1171G>T

Select item 14799930166.

rs1479993016 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:31472152 (GRCh38)
6:31439929 (GRCh37)
Canonical SPDI:: NC_000006.12:31472151:G:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31472152G>T, NC_000006.11:g.31439929G>T, NT_113891.3:g.2949477G>T, NT_113891.2:g.2949583G>T, NT_167248.2:g.2728039G>T, NT_167248.1:g.2733635G>T, NT_167245.2:g.2719678G>T, NT_167245.1:g.2725263G>T, NT_167249.2:g.2771397G>T, NT_167249.1:g.2770695G>T, NT_167247.2:g.2814124G>T, NT_167247.1:g.2819709G>T, NR_002812.3:n.924G>T

Select item 14786048947.

rs1478604894 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 6:31471273 (GRCh38)
6:31439050 (GRCh37)
Canonical SPDI:: NC_000006.12:31471272:G:A,NC_000006.12:31471272:G:C
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000006.12:g.31471273G>A, NC_000006.12:g.31471273G>C, NC_000006.11:g.31439050G>A, NC_000006.11:g.31439050G>C, NT_113891.3:g.2948598G>A, NT_113891.3:g.2948598G>C, NT_113891.2:g.2948704G>A, NT_113891.2:g.2948704G>C, NT_167248.2:g.2727160G>A, NT_167248.2:g.2727160G>C, NT_167248.1:g.2732756G>A, NT_167248.1:g.2732756G>C, NT_167245.2:g.2718799G>A, NT_167245.2:g.2718799G>C, NT_167245.1:g.2724384G>A, NT_167245.1:g.2724384G>C, NT_167249.2:g.2770518G>A, NT_167249.2:g.2770518G>C, NT_167249.1:g.2769816G>A, NT_167249.1:g.2769816G>C, NT_167247.2:g.2813245G>A, NT_167247.2:g.2813245G>C, NT_167247.1:g.2818830G>A, NT_167247.1:g.2818830G>C, NR_002812.3:n.45G>A, NR_002812.3:n.45G>C

Select item 14785937158.

rs1478593715 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31472333 (GRCh38)
6:31440110 (GRCh37)
Canonical SPDI:: NC_000006.12:31472332:G:A
Gene:: HCG26 (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=0.000035/1 (TOMMO)
HGVS:: NC_000006.12:g.31472333G>A, NC_000006.11:g.31440110G>A, NT_113891.3:g.2949658G>A, NT_113891.2:g.2949764G>A, NT_167248.2:g.2728220G>A, NT_167248.1:g.2733816G>A, NT_167245.2:g.2719859G>A, NT_167245.1:g.2725444G>A, NT_167249.2:g.2771578G>A, NT_167249.1:g.2770876G>A, NT_167247.2:g.2814305G>A, NT_167247.1:g.2819890G>A, NR_002812.3:n.1105G>A

Select item 14785445879.

rs1478544587 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATGTTA>- [Show Flanks]
Chromosome:: 6:31472222 (GRCh38)
6:31439999 (GRCh37)
Canonical SPDI:: NC_000006.12:31472220:AATGTTA:A
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31472222_31472227del, NC_000006.11:g.31439999_31440004del, NT_113891.3:g.2949547_2949552del, NT_113891.2:g.2949653_2949658del, NT_167248.2:g.2728109_2728114del, NT_167248.1:g.2733705_2733710del, NT_167245.2:g.2719748_2719753del, NT_167245.1:g.2725333_2725338del, NT_167249.2:g.2771467_2771472del, NT_167249.1:g.2770765_2770770del, NT_167247.2:g.2814194_2814199del, NT_167247.1:g.2819779_2819784del, NR_002812.3:n.994_999del

Select item 147663570810.

rs1476635708 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31471371 (GRCh38)
6:31439148 (GRCh37)
Canonical SPDI:: NC_000006.12:31471370:C:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.022256/264 (ALFA)
T=0.000032/4 (GnomAD)
T=0.000142/4 (TOMMO)
T=0.000468/3 (1000Genomes)
HGVS:: NC_000006.12:g.31471371C>T, NC_000006.11:g.31439148C>T, NT_113891.3:g.2948696C>T, NT_113891.2:g.2948802C>T, NT_167248.2:g.2727258C>T, NT_167248.1:g.2732854C>T, NT_167245.2:g.2718897C>T, NT_167245.1:g.2724482C>T, NT_167249.2:g.2770616C>T, NT_167249.1:g.2769914C>T, NT_167247.2:g.2813343C>T, NT_167247.1:g.2818928C>T, NR_002812.3:n.143C>T

Select item 147585075311.

rs1475850753 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:31471261 (GRCh38)
6:31439038 (GRCh37)
Canonical SPDI:: NC_000006.12:31471260:G:A,NC_000006.12:31471260:G:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.31471261G>A, NC_000006.12:g.31471261G>T, NC_000006.11:g.31439038G>A, NC_000006.11:g.31439038G>T, NT_113891.3:g.2948586G>A, NT_113891.3:g.2948586G>T, NT_113891.2:g.2948692G>A, NT_113891.2:g.2948692G>T, NT_167248.2:g.2727148G>A, NT_167248.2:g.2727148G>T, NT_167248.1:g.2732744G>A, NT_167248.1:g.2732744G>T, NT_167245.2:g.2718787G>A, NT_167245.2:g.2718787G>T, NT_167245.1:g.2724372G>A, NT_167245.1:g.2724372G>T, NT_167249.2:g.2770506G>A, NT_167249.2:g.2770506G>T, NT_167249.1:g.2769804G>A, NT_167249.1:g.2769804G>T, NT_167247.2:g.2813233G>A, NT_167247.2:g.2813233G>T, NT_167247.1:g.2818818G>A, NT_167247.1:g.2818818G>T, NR_002812.3:n.33G>A, NR_002812.3:n.33G>T

Select item 147276161312.

rs1472761613 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31471375 (GRCh38)
6:31439152 (GRCh37)
Canonical SPDI:: NC_000006.12:31471374:A:G
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.022172/263 (ALFA)
G=0.00004/5 (GnomAD)
G=0.000142/4 (TOMMO)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000006.12:g.31471375A>G, NC_000006.11:g.31439152A>G, NT_113891.3:g.2948700A>G, NT_113891.2:g.2948806A>G, NT_167248.2:g.2727262A>G, NT_167248.1:g.2732858A>G, NT_167245.2:g.2718901A>G, NT_167245.1:g.2724486A>G, NT_167249.2:g.2770620A>G, NT_167249.1:g.2769918A>G, NT_167247.2:g.2813347A>G, NT_167247.1:g.2818932A>G, NR_002812.3:n.147A>G

Select item 147274855113.

rs1472748551 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31471709 (GRCh38)
6:31439486 (GRCh37)
Canonical SPDI:: NC_000006.12:31471708:A:G
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31471709A>G, NC_000006.11:g.31439486A>G, NT_113891.3:g.2949034A>G, NT_113891.2:g.2949140A>G, NT_167248.2:g.2727596A>G, NT_167248.1:g.2733192A>G, NT_167245.2:g.2719235A>G, NT_167245.1:g.2724820A>G, NT_167249.2:g.2770954A>G, NT_167249.1:g.2770252A>G, NT_167247.2:g.2813681A>G, NT_167247.1:g.2819266A>G, NR_002812.3:n.481A>G

Select item 146948557214.

rs1469485572 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31472111 (GRCh38)
6:31439888 (GRCh37)
Canonical SPDI:: NC_000006.12:31472110:A:G
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.31472111A>G, NC_000006.11:g.31439888A>G, NT_113891.3:g.2949436A>G, NT_113891.2:g.2949542A>G, NT_167248.2:g.2727998A>G, NT_167248.1:g.2733594A>G, NT_167245.2:g.2719637A>G, NT_167245.1:g.2725222A>G, NT_167249.2:g.2771356A>G, NT_167249.1:g.2770654A>G, NT_167247.2:g.2814083A>G, NT_167247.1:g.2819668A>G, NR_002812.3:n.883A>G

Select item 146905699615.

rs1469056996 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31472041 (GRCh38)
6:31439818 (GRCh37)
Canonical SPDI:: NC_000006.12:31472040:G:A
Gene:: HCG26 (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_000006.12:g.31472041G>A, NC_000006.11:g.31439818G>A, NT_113891.3:g.2949366G>A, NT_113891.2:g.2949472G>A, NT_167248.2:g.2727928G>A, NT_167248.1:g.2733524G>A, NT_167245.2:g.2719567G>A, NT_167245.1:g.2725152G>A, NT_167249.2:g.2771286G>A, NT_167249.1:g.2770584G>A, NT_167247.2:g.2814013G>A, NT_167247.1:g.2819598G>A, NR_002812.3:n.813G>A

Select item 146531095416.

rs1465310954 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 6:31471973 (GRCh38)
6:31439750 (GRCh37)
Canonical SPDI:: NC_000006.12:31471972:GGG:GG
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
-=0.000021/3 (GnomAD)
-=0.000034/9 (TOPMED)
HGVS:: NC_000006.12:g.31471975del, NC_000006.11:g.31439752del, NT_113891.3:g.2949300del, NT_113891.2:g.2949406del, NT_167248.2:g.2727862del, NT_167248.1:g.2733458del, NT_167245.2:g.2719501del, NT_167245.1:g.2725086del, NT_167249.2:g.2771220del, NT_167249.1:g.2770518del, NT_167247.2:g.2813947del, NT_167247.1:g.2819532del, NR_002812.3:n.747del

Select item 146362502117.

rs1463625021 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:31471910 (GRCh38)
6:31439687 (GRCh37)
Canonical SPDI:: NC_000006.12:31471909:A:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.0004/2 (ALFA)
T=0.0004/2 (Estonian)
HGVS:: NC_000006.12:g.31471910A>T, NC_000006.11:g.31439687A>T, NT_113891.3:g.2949235A>T, NT_113891.2:g.2949341A>T, NT_167248.2:g.2727797A>T, NT_167248.1:g.2733393A>T, NT_167245.2:g.2719436A>T, NT_167245.1:g.2725021A>T, NT_167249.2:g.2771155A>T, NT_167249.1:g.2770453A>T, NT_167247.2:g.2813882A>T, NT_167247.1:g.2819467A>T, NR_002812.3:n.682A>T

Select item 145853028318.

rs1458530283 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31471387 (GRCh38)
6:31439164 (GRCh37)
Canonical SPDI:: NC_000006.12:31471386:A:G
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.04055/481 (ALFA)
G=0.000227/27 (GnomAD)
G=0.001093/7 (1000Genomes)
G=0.003506/99 (TOMMO)
HGVS:: NC_000006.12:g.31471387A>G, NC_000006.11:g.31439164A>G, NT_113891.3:g.2948712A>G, NT_113891.2:g.2948818A>G, NT_167248.2:g.2727274A>G, NT_167248.1:g.2732870A>G, NT_167245.2:g.2718913A>G, NT_167245.1:g.2724498A>G, NT_167249.2:g.2770632A>G, NT_167249.1:g.2769930A>G, NT_167247.2:g.2813359A>G, NT_167247.1:g.2818944A>G, NR_002812.3:n.159A>G

Select item 145842823819.

rs1458428238 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31471993 (GRCh38)
6:31439770 (GRCh37)
Canonical SPDI:: NC_000006.12:31471992:C:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31471993C>T, NC_000006.11:g.31439770C>T, NT_113891.3:g.2949318C>T, NT_113891.2:g.2949424C>T, NT_167248.2:g.2727880C>T, NT_167248.1:g.2733476C>T, NT_167245.2:g.2719519C>T, NT_167245.1:g.2725104C>T, NT_167249.2:g.2771238C>T, NT_167249.1:g.2770536C>T, NT_167247.2:g.2813965C>T, NT_167247.1:g.2819550C>T, NR_002812.3:n.765C>T

Select item 145557081320.

rs1455570813 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:31472157 (GRCh38)
6:31439934 (GRCh37)
Canonical SPDI:: NC_000006.12:31472156:G:A,NC_000006.12:31472156:G:T
Gene:: HCG26 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00016/1 (1000Genomes)
HGVS:: NC_000006.12:g.31472157G>A, NC_000006.12:g.31472157G>T, NC_000006.11:g.31439934G>A, NC_000006.11:g.31439934G>T, NT_113891.3:g.2949482G>A, NT_113891.3:g.2949482G>T, NT_113891.2:g.2949588G>A, NT_113891.2:g.2949588G>T, NT_167248.2:g.2728044G>A, NT_167248.2:g.2728044G>T, NT_167248.1:g.2733640G>A, NT_167248.1:g.2733640G>T, NT_167245.2:g.2719683G>A, NT_167245.2:g.2719683G>T, NT_167245.1:g.2725268G>A, NT_167245.1:g.2725268G>T, NT_167249.2:g.2771402G>A, NT_167249.2:g.2771402G>T, NT_167249.1:g.2770700G>A, NT_167249.1:g.2770700G>T, NT_167247.2:g.2814129G>A, NT_167247.2:g.2814129G>T, NT_167247.1:g.2819714G>A, NT_167247.1:g.2819714G>T, NR_002812.3:n.929G>A, NR_002812.3:n.929G>T

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 243

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity