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Select item 14875543511.

rs1487554351 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:116169443 (GRCh38)
X:115300696 (GRCh37)
Canonical SPDI:: NC_000023.11:116169442:G:A
Gene:: AGTR2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000023.11:g.116169443G>A, NC_000023.10:g.115300696G>A, NG_016326.1:g.3739G>A, NW_004070892.1:g.330494G>A

Select item 14874117112.

rs1487411711 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:116175329 (GRCh38)
X:115306582 (GRCh37)
Canonical SPDI:: NC_000023.11:116175328:C:G
Gene:: AGTR2 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.116175329C>G, NC_000023.10:g.115306582C>G, NG_016326.1:g.9625C>G, NW_004070892.1:g.336380C>G

Select item 14870143013.

rs1487014301 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:116172608 (GRCh38)
X:115303861 (GRCh37)
Canonical SPDI:: NC_000023.11:116172607:T:G
Gene:: AGTR2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.116172608T>G, NC_000023.10:g.115303861T>G, NG_016326.1:g.6904T>G, NM_000686.5:c.328T>G, NM_000686.4:c.328T>G, NM_001385624.1:c.328T>G, NW_004070892.1:g.333659T>G, NP_000677.2:p.Trp110Gly, NP_001372553.1:p.Trp110Gly

Select item 14867147484.

rs1486714748 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:116173746 (GRCh38)
X:115304999 (GRCh37)
Canonical SPDI:: NC_000023.11:116173745:C:T
Gene:: AGTR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.116173746C>T, NC_000023.10:g.115304999C>T, NG_016326.1:g.8042C>T, NM_000686.5:c.*374C>T, NM_000686.4:c.*374C>T, NM_001385624.1:c.*374C>T, NW_004070892.1:g.334797C>T

Select item 14866734335.

rs1486673433 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:116174468 (GRCh38)
X:115305721 (GRCh37)
Canonical SPDI:: NC_000023.11:116174467:A:G
Gene:: AGTR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000023.11:g.116174468A>G, NC_000023.10:g.115305721A>G, NG_016326.1:g.8764A>G, NM_000686.5:c.*1096A>G, NM_000686.4:c.*1096A>G, NM_001385624.1:c.*1096A>G, NW_004070892.1:g.335519A>G

Select item 14857315606.

rs1485731560 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:116174633 (GRCh38)
X:115305886 (GRCh37)
Canonical SPDI:: NC_000023.11:116174632:G:A
Gene:: AGTR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000034/9 (TOPMED)
HGVS:: NC_000023.11:g.116174633G>A, NC_000023.10:g.115305886G>A, NG_016326.1:g.8929G>A, NM_000686.5:c.*1261G>A, NM_000686.4:c.*1261G>A, NM_001385624.1:c.*1261G>A, NW_004070892.1:g.335684G>A

Select item 14855266367.

rs1485526636 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:116170498 (GRCh38)
X:115301751 (GRCh37)
Canonical SPDI:: NC_000023.11:116170497:A:G
Gene:: AGTR2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.116170498A>G, NC_000023.10:g.115301751A>G, NG_016326.1:g.4794A>G, NW_004070892.1:g.331549A>G

Select item 14851692058.

rs1485169205 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:116171296 (GRCh38)
X:115302549 (GRCh37)
Canonical SPDI:: NC_000023.11:116171295:T:C
Gene:: AGTR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000076/20 (TOPMED)
C=0.000147/15 (GnomAD)
HGVS:: NC_000023.11:g.116171296T>C, NC_000023.10:g.115302549T>C, NG_016326.1:g.5592T>C, NW_004070892.1:g.332347T>C

Select item 14831286289.

rs1483128628 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:116169755 (GRCh38)
X:115301008 (GRCh37)
Canonical SPDI:: NC_000023.11:116169754:A:G
Gene:: AGTR2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.116169755A>G, NC_000023.10:g.115301008A>G, NG_016326.1:g.4051A>G, NW_004070892.1:g.330806A>G

Select item 148287722210.

rs1482877222 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:116169250 (GRCh38)
X:115300503 (GRCh37)
Canonical SPDI:: NC_000023.11:116169249:G:A
Gene:: AGTR2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.116169250G>A, NC_000023.10:g.115300503G>A, NG_016326.1:g.3546G>A, NW_004070892.1:g.330301G>A

Select item 148189323211.

rs1481893232 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:116169932 (GRCh38)
X:115301185 (GRCh37)
Canonical SPDI:: NC_000023.11:116169931:T:C
Gene:: AGTR2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000048/5 (GnomAD)
HGVS:: NC_000023.11:g.116169932T>C, NC_000023.10:g.115301185T>C, NG_016326.1:g.4228T>C, NW_004070892.1:g.330983T>C

Select item 148063480412.

rs1480634804 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: X:116169432 (GRCh38)
X:115300685 (GRCh37)
Canonical SPDI:: NC_000023.11:116169430:TGT:T
Gene:: AGTR2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.116169432_116169433del, NC_000023.10:g.115300685_115300686del, NG_016326.1:g.3728_3729del, NW_004070892.1:g.330483_330484del

Select item 148036337613.

rs1480363376 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:116170840 (GRCh38)
X:115302093 (GRCh37)
Canonical SPDI:: NC_000023.11:116170839:A:G
Gene:: AGTR2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.00001/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.116170840A>G, NC_000023.10:g.115302093A>G, NG_016326.1:g.5136A>G, NW_004070892.1:g.331891A>G

Select item 147919511514.

rs1479195115 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:116168729 (GRCh38)
X:115299982 (GRCh37)
Canonical SPDI:: NC_000023.11:116168728:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000142/2 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.116168729G>C, NC_000023.10:g.115299982G>C, NG_016326.1:g.3025G>C, NW_004070892.1:g.329780G>C

Select item 147890577915.

rs1478905779 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:116175117 (GRCh38)
X:115306370 (GRCh37)
Canonical SPDI:: NC_000023.11:116175116:C:G
Gene:: AGTR2 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.116175117C>G, NC_000023.10:g.115306370C>G, NG_016326.1:g.9413C>G, NW_004070892.1:g.336168C>G

Select item 147878128316.

rs1478781283 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:116170272 (GRCh38)
X:115301525 (GRCh37)
Canonical SPDI:: NC_000023.11:116170271:C:G
Gene:: AGTR2 (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=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.116170272C>G, NC_000023.10:g.115301525C>G, NG_016326.1:g.4568C>G, NW_004070892.1:g.331323C>G

Select item 147733622317.

rs1477336223 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:116173732 (GRCh38)
X:115304985 (GRCh37)
Canonical SPDI:: NC_000023.11:116173731:T:C
Gene:: AGTR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.116173732T>C, NC_000023.10:g.115304985T>C, NG_016326.1:g.8028T>C, NM_000686.5:c.*360T>C, NM_000686.4:c.*360T>C, NM_001385624.1:c.*360T>C, NW_004070892.1:g.334783T>C

Select item 147699594518.

rs1476995945 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:116175413 (GRCh38)
X:115306666 (GRCh37)
Canonical SPDI:: NC_000023.11:116175412:A:G
Gene:: AGTR2 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.116175413A>G, NC_000023.10:g.115306666A>G, NG_016326.1:g.9709A>G, NW_004070892.1:g.336464A>G

Select item 147633587419.

rs1476335874 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:116173915 (GRCh38)
X:115305168 (GRCh37)
Canonical SPDI:: NC_000023.11:116173914:T:C
Gene:: AGTR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000045/12 (TOPMED)
C=0.000058/6 (GnomAD)
HGVS:: NC_000023.11:g.116173915T>C, NC_000023.10:g.115305168T>C, NG_016326.1:g.8211T>C, NM_000686.5:c.*543T>C, NM_000686.4:c.*543T>C, NM_001385624.1:c.*543T>C, NW_004070892.1:g.334966T>C

Select item 147563722920.

rs1475637229 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:116173579 (GRCh38)
X:115304832 (GRCh37)
Canonical SPDI:: NC_000023.11:116173578:T:C
Gene:: AGTR2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000019/2 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.116173579T>C, NC_000023.10:g.115304832T>C, NG_016326.1:g.7875T>C, NM_000686.5:c.*207T>C, NM_000686.4:c.*207T>C, NM_001385624.1:c.*207T>C, NW_004070892.1:g.334630T>C

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