rs121918588

Orientation

minus

Stabilized

minus

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

Make rs121918588(G;T)

Make rs121918588(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

49636810

Gene

RHAG

is a	snp
is	mentioned by
dbSNP	rs121918588
dbSNP (classic)	rs121918588
ClinGen	rs121918588
ebi	rs121918588
HLI	rs121918588
Exac	rs121918588
Gnomad	rs121918588
Varsome	rs121918588
LitVar	rs121918588
Map	rs121918588
PheGenI	rs121918588
Biobank	rs121918588
1000 genomes	rs121918588
hgdp	rs121918588
ensembl	rs121918588
geneview	rs121918588
scholar	rs121918588
google	rs121918588
pharmgkb	rs121918588
gwascentral	rs121918588
openSNP	rs121918588
23andMe	rs121918588
SNPshot	rs121918588
SNPdbe	rs121918588
MSV3d	rs121918588
GWAS Ctlg	rs121918588

Max Magnitude

0

OMIM	180297
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121918588(T;T)
Alt	rs121918588(T;T)
Reference	Rs121918588(G;G)
Significance	Pathogenic
Disease	Rh-mod syndrome
Variation	info
Gene	RHAG
CLNDBN	Rh-mod syndrome
Reversed	1
HGVS	NC_000006.11:g.49604523C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013938.25,