rs16879498

Orientation

plus

Stabilized

plus

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

Make rs16879498(C;T)

Make rs16879498(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

49612534

Gene

RHAG

is a	snp
is	mentioned by
dbSNP	rs16879498
dbSNP (classic)	rs16879498
ClinGen	rs16879498
ebi	rs16879498
HLI	rs16879498
Exac	rs16879498
Gnomad	rs16879498
Varsome	rs16879498
LitVar	rs16879498
Map	rs16879498
PheGenI	rs16879498
Biobank	rs16879498
1000 genomes	rs16879498
hgdp	rs16879498
ensembl	rs16879498
geneview	rs16879498
scholar	rs16879498
google	rs16879498
pharmgkb	rs16879498
gwascentral	rs16879498
openSNP	rs16879498
23andMe	rs16879498
SNPshot	rs16879498
SNPdbe	rs16879498
MSV3d	rs16879498
GWAS Ctlg	rs16879498

GMAF

0.05142

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

OMIM	180297
Desc	RH-NULL HEMOLYTIC ANEMIA, REGULATOR TYPE
Variant	0009
Related	also

ClinVar
Risk	rs16879498(T;T)
Alt	rs16879498(T;T)
Reference	Rs16879498(C;C)
Significance	Pathogenic
Disease	Rh-null hemolytic anemia Rh-null
Variation	info
Gene	RHAG
CLNDBN	Rh-null hemolytic anemia, regulator type Rh-null, regulator type
Reversed	0
HGVS	NC_000006.11:g.49580247C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013940.25, RCV000490272.1,