SNP Links for Nucleotide (Select 224994165) - SNP

Links from Nucleotide

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Select item 14915361171.

rs1491536117 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:55681887 (GRCh38)
7:55749580 (GRCh37)
Canonical SPDI:: NC_000007.14:55681886:CA:
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000007.14:g.55681887_55681888del, NC_000007.13:g.55749580_55749581del, NR_027339.1:n.1727_1728del, NR_027342.1:n.1637_1638del, NR_003949.1:n.1623_1624del, NR_027340.1:n.1356_1357del

Select item 14911313542.

rs1491131354 has merged into rs59524171 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 7:55681897 (GRCh38)
7:55749590 (GRCh37)
Canonical SPDI:: NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:55681887:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.55681897_55681909del, NC_000007.14:g.55681898_55681909del, NC_000007.14:g.55681899_55681909del, NC_000007.14:g.55681900_55681909del, NC_000007.14:g.55681901_55681909del, NC_000007.14:g.55681902_55681909del, NC_000007.14:g.55681903_55681909del, NC_000007.14:g.55681904_55681909del, NC_000007.14:g.55681905_55681909del, NC_000007.14:g.55681906_55681909del, NC_000007.14:g.55681907_55681909del, NC_000007.14:g.55681908_55681909del, NC_000007.14:g.55681909del, NC_000007.14:g.55681909dup, NC_000007.14:g.55681908_55681909dup, NC_000007.14:g.55681907_55681909dup, NC_000007.14:g.55681906_55681909dup, NC_000007.14:g.55681905_55681909dup, NC_000007.14:g.55681904_55681909dup, NC_000007.14:g.55681901_55681909dup, NC_000007.14:g.55681900_55681909dup, NC_000007.13:g.55749590_55749602del, NC_000007.13:g.55749591_55749602del, NC_000007.13:g.55749592_55749602del, NC_000007.13:g.55749593_55749602del, NC_000007.13:g.55749594_55749602del, NC_000007.13:g.55749595_55749602del, NC_000007.13:g.55749596_55749602del, NC_000007.13:g.55749597_55749602del, NC_000007.13:g.55749598_55749602del, NC_000007.13:g.55749599_55749602del, NC_000007.13:g.55749600_55749602del, NC_000007.13:g.55749601_55749602del, NC_000007.13:g.55749602del, NC_000007.13:g.55749602dup, NC_000007.13:g.55749601_55749602dup, NC_000007.13:g.55749600_55749602dup, NC_000007.13:g.55749599_55749602dup, NC_000007.13:g.55749598_55749602dup, NC_000007.13:g.55749597_55749602dup, NC_000007.13:g.55749594_55749602dup, NC_000007.13:g.55749593_55749602dup, NR_027339.1:n.1715_1727del, NR_027339.1:n.1716_1727del, NR_027339.1:n.1717_1727del, NR_027339.1:n.1718_1727del, NR_027339.1:n.1719_1727del, NR_027339.1:n.1720_1727del, NR_027339.1:n.1721_1727del, NR_027339.1:n.1722_1727del, NR_027339.1:n.1723_1727del, NR_027339.1:n.1724_1727del, NR_027339.1:n.1725_1727del, NR_027339.1:n.1726_1727del, NR_027339.1:n.1727del, NR_027339.1:n.1727dup, NR_027339.1:n.1726_1727dup, NR_027339.1:n.1725_1727dup, NR_027339.1:n.1724_1727dup, NR_027339.1:n.1723_1727dup, NR_027339.1:n.1722_1727dup, NR_027339.1:n.1719_1727dup, NR_027339.1:n.1718_1727dup, NR_027342.1:n.1625_1637del, NR_027342.1:n.1626_1637del, NR_027342.1:n.1627_1637del, NR_027342.1:n.1628_1637del, NR_027342.1:n.1629_1637del, NR_027342.1:n.1630_1637del, NR_027342.1:n.1631_1637del, NR_027342.1:n.1632_1637del, NR_027342.1:n.1633_1637del, NR_027342.1:n.1634_1637del, NR_027342.1:n.1635_1637del, NR_027342.1:n.1636_1637del, NR_027342.1:n.1637del, NR_027342.1:n.1637dup, NR_027342.1:n.1636_1637dup, NR_027342.1:n.1635_1637dup, NR_027342.1:n.1634_1637dup, NR_027342.1:n.1633_1637dup, NR_027342.1:n.1632_1637dup, NR_027342.1:n.1629_1637dup, NR_027342.1:n.1628_1637dup, NR_003949.1:n.1611_1623del, NR_003949.1:n.1612_1623del, NR_003949.1:n.1613_1623del, NR_003949.1:n.1614_1623del, NR_003949.1:n.1615_1623del, NR_003949.1:n.1616_1623del, NR_003949.1:n.1617_1623del, NR_003949.1:n.1618_1623del, NR_003949.1:n.1619_1623del, NR_003949.1:n.1620_1623del, NR_003949.1:n.1621_1623del, NR_003949.1:n.1622_1623del, NR_003949.1:n.1623del, NR_003949.1:n.1623dup, NR_003949.1:n.1622_1623dup, NR_003949.1:n.1621_1623dup, NR_003949.1:n.1620_1623dup, NR_003949.1:n.1619_1623dup, NR_003949.1:n.1618_1623dup, NR_003949.1:n.1615_1623dup, NR_003949.1:n.1614_1623dup, NR_027340.1:n.1344_1356del, NR_027340.1:n.1345_1356del, NR_027340.1:n.1346_1356del, NR_027340.1:n.1347_1356del, NR_027340.1:n.1348_1356del, NR_027340.1:n.1349_1356del, NR_027340.1:n.1350_1356del, NR_027340.1:n.1351_1356del, NR_027340.1:n.1352_1356del, NR_027340.1:n.1353_1356del, NR_027340.1:n.1354_1356del, NR_027340.1:n.1355_1356del, NR_027340.1:n.1356del, NR_027340.1:n.1356dup, NR_027340.1:n.1355_1356dup, NR_027340.1:n.1354_1356dup, NR_027340.1:n.1353_1356dup, NR_027340.1:n.1352_1356dup, NR_027340.1:n.1351_1356dup, NR_027340.1:n.1348_1356dup, NR_027340.1:n.1347_1356dup, NM_182827.1:c.*750_*762del, NM_182827.1:c.*751_*762del, NM_182827.1:c.*752_*762del, NM_182827.1:c.*753_*762del, NM_182827.1:c.*754_*762del, NM_182827.1:c.*755_*762del, NM_182827.1:c.*756_*762del, NM_182827.1:c.*757_*762del, NM_182827.1:c.*758_*762del, NM_182827.1:c.*759_*762del, NM_182827.1:c.*760_*762del, NM_182827.1:c.*761_*762del, NM_182827.1:c.*762del, NM_182827.1:c.*762dup, NM_182827.1:c.*761_*762dup, NM_182827.1:c.*760_*762dup, NM_182827.1:c.*759_*762dup, NM_182827.1:c.*758_*762dup, NM_182827.1:c.*757_*762dup, NM_182827.1:c.*754_*762dup, NM_182827.1:c.*753_*762dup

Select item 14907954653.

rs1490795465 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:55681105 (GRCh38)
7:55748798 (GRCh37)
Canonical SPDI:: NC_000007.14:55681104:A:G
Gene:: FKBP9P1 (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_000007.14:g.55681105A>G, NC_000007.13:g.55748798A>G, NR_027339.1:n.2510T>C, NR_027342.1:n.2420T>C, NR_003949.1:n.2406T>C, NR_027340.1:n.2139T>C, NM_182827.1:c.*1545T>C

Select item 14907232144.

rs1490723214 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:55682798 (GRCh38)
7:55750491 (GRCh37)
Canonical SPDI:: NC_000007.14:55682797:C:G
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.55682798C>G, NC_000007.13:g.55750491C>G, NR_027339.1:n.817G>C, NR_027342.1:n.727G>C, NR_003949.1:n.713G>C, NR_027340.1:n.446G>C, NM_182827.1:c.280G>C

Select item 14896622845.

rs1489662284 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:55689218 (GRCh38)
7:55756911 (GRCh37)
Canonical SPDI:: NC_000007.14:55689217:C:G,NC_000007.14:55689217:C:T
Gene:: FKBP9P1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000007.14:g.55689218C>G, NC_000007.14:g.55689218C>T, NC_000007.13:g.55756911C>G, NC_000007.13:g.55756911C>T, NR_027339.1:n.243G>C, NR_027339.1:n.243G>A, NR_027342.1:n.84G>C, NR_027342.1:n.84G>A, NM_182827.1:c.-364G>C, NM_182827.1:c.-364G>A

Select item 14888113076.

rs1488811307 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:55682124 (GRCh38)
7:55749817 (GRCh37)
Canonical SPDI:: NC_000007.14:55682123:T:C
Gene:: FKBP9P1 (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_000007.14:g.55682124T>C, NC_000007.13:g.55749817T>C, NR_027339.1:n.1491A>G, NR_027342.1:n.1401A>G, NR_003949.1:n.1387A>G, NR_027340.1:n.1120A>G, NM_182827.1:c.*525A>G

Select item 14882012527.

rs1488201252 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:55681556 (GRCh38)
7:55749249 (GRCh37)
Canonical SPDI:: NC_000007.14:55681555:G:A
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.55681556G>A, NC_000007.13:g.55749249G>A, NR_027339.1:n.2059C>T, NR_027342.1:n.1969C>T, NR_003949.1:n.1955C>T, NR_027340.1:n.1688C>T, NM_182827.1:c.*1094C>T

Select item 14878057408.

rs1487805740 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:55681566 (GRCh38)
7:55749259 (GRCh37)
Canonical SPDI:: NC_000007.14:55681565:G:A
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000029/4 (GnomAD)
A=0.000064/17 (TOPMED)
HGVS:: NC_000007.14:g.55681566G>A, NC_000007.13:g.55749259G>A, NR_027339.1:n.2049C>T, NR_027342.1:n.1959C>T, NR_003949.1:n.1945C>T, NR_027340.1:n.1678C>T, NM_182827.1:c.*1084C>T

Select item 14877939599.

rs1487793959 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:55689015 (GRCh38)
7:55756708 (GRCh37)
Canonical SPDI:: NC_000007.14:55689014:A:G
Gene:: FKBP9P1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_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_000007.14:g.55689015A>G, NC_000007.13:g.55756708A>G, NR_027339.1:n.446T>C, NR_027342.1:n.287T>C, NM_182827.1:c.-161T>C

Select item 148775413610.

rs1487754136 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 7:55682113 (GRCh38)
7:55749806 (GRCh37)
Canonical SPDI:: NC_000007.14:55682112:T:C,NC_000007.14:55682112:T:G
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
G=0.001092/2 (Korea1K)
HGVS:: NC_000007.14:g.55682113T>C, NC_000007.14:g.55682113T>G, NC_000007.13:g.55749806T>C, NC_000007.13:g.55749806T>G, NR_027339.1:n.1502A>G, NR_027339.1:n.1502A>C, NR_027342.1:n.1412A>G, NR_027342.1:n.1412A>C, NR_003949.1:n.1398A>G, NR_003949.1:n.1398A>C, NR_027340.1:n.1131A>G, NR_027340.1:n.1131A>C, NM_182827.1:c.*536A>G, NM_182827.1:c.*536A>C

Select item 148742636511.

rs1487426365 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:55681345 (GRCh38)
7:55749038 (GRCh37)
Canonical SPDI:: NC_000007.14:55681344:C:T
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.55681345C>T, NC_000007.13:g.55749038C>T, NR_027339.1:n.2270G>A, NR_027342.1:n.2180G>A, NR_003949.1:n.2166G>A, NR_027340.1:n.1899G>A, NM_182827.1:c.*1305G>A

Select item 148208209712.

rs1482082097 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:55682104 (GRCh38)
7:55749797 (GRCh37)
Canonical SPDI:: NC_000007.14:55682103:G:C
Gene:: FKBP9P1 (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_000007.14:g.55682104G>C, NC_000007.13:g.55749797G>C, NR_027339.1:n.1511C>G, NR_027342.1:n.1421C>G, NR_003949.1:n.1407C>G, NR_027340.1:n.1140C>G, NM_182827.1:c.*545C>G

Select item 148197399813.

rs1481973998 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:55681390 (GRCh38)
7:55749083 (GRCh37)
Canonical SPDI:: NC_000007.14:55681389:G:A
Gene:: FKBP9P1 (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_000007.14:g.55681390G>A, NC_000007.13:g.55749083G>A, NR_027339.1:n.2225C>T, NR_027342.1:n.2135C>T, NR_003949.1:n.2121C>T, NR_027340.1:n.1854C>T, NM_182827.1:c.*1260C>T

Select item 147886740114.

rs1478867401 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 7:55681906 (GRCh38)
7:55749600 (GRCh37)
Canonical SPDI:: NC_000007.14:55681906::G
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000843/10 (ALFA)
G=0.001677/233 (GnomAD)
HGVS:: NC_000007.14:g.55681906_55681907insG, NC_000007.13:g.55749599_55749600insG, NR_027339.1:n.1708_1709insC, NR_027342.1:n.1618_1619insC, NR_003949.1:n.1604_1605insC, NR_027340.1:n.1337_1338insC, NM_182827.1:c.*742_*743insC

Select item 147685041415.

rs1476850414 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:55681179 (GRCh38)
7:55748872 (GRCh37)
Canonical SPDI:: NC_000007.14:55681178:A:G
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.55681179A>G, NC_000007.13:g.55748872A>G, NR_027339.1:n.2436T>C, NR_027342.1:n.2346T>C, NR_003949.1:n.2332T>C, NR_027340.1:n.2065T>C, NM_182827.1:c.*1471T>C

Select item 147496453016.

rs1474964530 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:55682691 (GRCh38)
7:55750384 (GRCh37)
Canonical SPDI:: NC_000007.14:55682690:T:G
Gene:: FKBP9P1 (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_000007.14:g.55682691T>G, NC_000007.13:g.55750384T>G, NR_027339.1:n.924A>C, NR_027342.1:n.834A>C, NR_003949.1:n.820A>C, NR_027340.1:n.553A>C, NM_182827.1:c.387A>C

Select item 147315011917.

rs1473150119 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:55682677 (GRCh38)
7:55750370 (GRCh37)
Canonical SPDI:: NC_000007.14:55682676:T:C
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.55682677T>C, NC_000007.13:g.55750370T>C, NR_027339.1:n.938A>G, NR_027342.1:n.848A>G, NR_003949.1:n.834A>G, NR_027340.1:n.567A>G, NM_182827.1:c.401A>G

Select item 147273717518.

rs1472737175 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:55681199 (GRCh38)
7:55748892 (GRCh37)
Canonical SPDI:: NC_000007.14:55681198:T:G
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.55681199T>G, NC_000007.13:g.55748892T>G, NR_027339.1:n.2416A>C, NR_027342.1:n.2326A>C, NR_003949.1:n.2312A>C, NR_027340.1:n.2045A>C, NM_182827.1:c.*1451A>C

Select item 147125540119.

rs1471255401 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:55685179 (GRCh38)
7:55752872 (GRCh37)
Canonical SPDI:: NC_000007.14:55685178:A:G
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000007.14:g.55685179A>G, NC_000007.13:g.55752872A>G, NR_027339.1:n.782T>C, NR_027342.1:n.692T>C, NR_003949.1:n.678T>C, NR_027340.1:n.411T>C, NM_182827.1:c.245T>C

Select item 147122946920.

rs1471229469 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:55682594 (GRCh38)
7:55750287 (GRCh37)
Canonical SPDI:: NC_000007.14:55682593:C:T
Gene:: FKBP9P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.55682594C>T, NC_000007.13:g.55750287C>T, NR_027339.1:n.1021G>A, NR_027342.1:n.931G>A, NR_003949.1:n.917G>A, NR_027340.1:n.650G>A, NM_182827.1:c.*55G>A

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