rs6478078

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(G;G)	0	common in clinvar

Make rs6478078(C;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

114404058

Gene

WHRN

is a	snp
is	mentioned by
dbSNP	rs6478078
dbSNP (classic)	rs6478078
ClinGen	rs6478078
ebi	rs6478078
HLI	rs6478078
Exac	rs6478078
Gnomad	rs6478078
Varsome	rs6478078
LitVar	rs6478078
Map	rs6478078
PheGenI	rs6478078
Biobank	rs6478078
1000 genomes	rs6478078
hgdp	rs6478078
ensembl	rs6478078
geneview	rs6478078
scholar	rs6478078
google	rs6478078
pharmgkb	rs6478078
gwascentral	rs6478078
openSNP	rs6478078
23andMe	rs6478078
SNPshot	rs6478078
SNPdbe	rs6478078
MSV3d	rs6478078
GWAS Ctlg	rs6478078

GMAF

0.003673

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

ClinVar
Risk	Rs6478078(C;C)
Alt	Rs6478078(C;C)
Reference	Rs6478078(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	WHRN DFNB31
CLNDBN	not specified
Reversed	0
HGVS	NC_000009.11:g.117166338G\x3d; NC_000009.11:g.117166338G>C
CLNSRC
CLNACC	RCV000154362.1, RCV000038886.2,