rs121917779

Orientation

minus

Stabilized

minus

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

Make rs121917779(A;C)

Make rs121917779(C;C)

Reference

GRCh38 38.1/141

Chromosome

5

Position

41201565

Gene

C6

is a	snp
is	mentioned by
dbSNP	rs121917779
dbSNP (classic)	rs121917779
ClinGen	rs121917779
ebi	rs121917779
HLI	rs121917779
Exac	rs121917779
Gnomad	rs121917779
Varsome	rs121917779
LitVar	rs121917779
Map	rs121917779
PheGenI	rs121917779
Biobank	rs121917779
1000 genomes	rs121917779
hgdp	rs121917779
ensembl	rs121917779
geneview	rs121917779
scholar	rs121917779
google	rs121917779
pharmgkb	rs121917779
gwascentral	rs121917779
openSNP	rs121917779
23andMe	rs121917779
SNPshot	rs121917779
SNPdbe	rs121917779
MSV3d	rs121917779
GWAS Ctlg	rs121917779

Max Magnitude

0

OMIM	217050
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121917779(C;C) rs121917779(G;G)
Alt	rs121917779(C;C) rs121917779(G;G)
Reference	Rs121917779(A;A)
Significance	Non-pathogenic
Disease	C6 A/B POLYMORPHISM
Variation	info
Gene	C6
CLNDBN	C6 A/B POLYMORPHISM
Reversed	1
HGVS	NC_000005.9:g.41201667T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012896.2,