rs774648934

Orientation

plus

Stabilized

plus

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

Make rs774648934(C;C)

Make rs774648934(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

80158085

Gene

FAH

is a	snp
is	mentioned by
dbSNP	rs774648934
dbSNP (classic)	rs774648934
ClinGen	rs774648934
ebi	rs774648934
HLI	rs774648934
Exac	rs774648934
Gnomad	rs774648934
Varsome	rs774648934
LitVar	rs774648934
Map	rs774648934
PheGenI	rs774648934
Biobank	rs774648934
1000 genomes	rs774648934
hgdp	rs774648934
ensembl	rs774648934
geneview	rs774648934
scholar	rs774648934
google	rs774648934
pharmgkb	rs774648934
gwascentral	rs774648934
openSNP	rs774648934
23andMe	rs774648934
SNPshot	rs774648934
SNPdbe	rs774648934
MSV3d	rs774648934
GWAS Ctlg	rs774648934

Max Magnitude

0

ClinVar
Risk	rs774648934(C;C)
Alt	rs774648934(C;C)
Reference	Rs774648934(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FAH
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.80450427T>C
CLNSRC
CLNACC	RCV000494624.1,