rs121918586

Orientation

minus

Stabilized

minus

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

Make rs121918586(A;A)

Make rs121918586(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

49619284

Gene

RHAG

is a	snp
is	mentioned by
dbSNP	rs121918586
dbSNP (classic)	rs121918586
ClinGen	rs121918586
ebi	rs121918586
HLI	rs121918586
Exac	rs121918586
Gnomad	rs121918586
Varsome	rs121918586
LitVar	rs121918586
Map	rs121918586
PheGenI	rs121918586
Biobank	rs121918586
1000 genomes	rs121918586
hgdp	rs121918586
ensembl	rs121918586
geneview	rs121918586
scholar	rs121918586
google	rs121918586
pharmgkb	rs121918586
gwascentral	rs121918586
openSNP	rs121918586
23andMe	rs121918586
SNPshot	rs121918586
SNPdbe	rs121918586
MSV3d	rs121918586
GWAS Ctlg	rs121918586

Max Magnitude

0

OMIM	180297
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918586(A;A) rs121918586(C;C)
Alt	rs121918586(A;A) rs121918586(C;C)
Reference	Rs121918586(G;G)
Significance	Pathogenic
Disease	Rh-null hemolytic anemia
Variation	info
Gene	RHAG
CLNDBN	Rh-null hemolytic anemia, regulator type
Reversed	1
HGVS	NC_000006.11:g.49586997C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013934.24,