rs121918362

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs121918362(G;T)

Make rs121918362(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

46501237

Gene

ZNF674

is a	snp
is	mentioned by
dbSNP	rs121918362
dbSNP (classic)	rs121918362
ClinGen	rs121918362
ebi	rs121918362
HLI	rs121918362
Exac	rs121918362
Gnomad	rs121918362
Varsome	rs121918362
LitVar	rs121918362
Map	rs121918362
PheGenI	rs121918362
Biobank	rs121918362
1000 genomes	rs121918362
hgdp	rs121918362
ensembl	rs121918362
geneview	rs121918362
scholar	rs121918362
google	rs121918362
pharmgkb	rs121918362
gwascentral	rs121918362
openSNP	rs121918362
23andMe	rs121918362
SNPshot	rs121918362
SNPdbe	rs121918362
MSV3d	rs121918362
GWAS Ctlg	rs121918362

Max Magnitude

0

OMIM	300573
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918362(T;T)
Alt	rs121918362(T;T)
Reference	Rs121918362(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ZNF674
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.46360672C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000088657.2,