rs1057517972

Orientation

plus

Stabilized

plus

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

Make rs1057517972(A;G)

Make rs1057517972(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

80153055

Gene

FAH

is a	snp
is	mentioned by
dbSNP	rs1057517972
dbSNP (classic)	rs1057517972
ClinGen	rs1057517972
ebi	rs1057517972
HLI	rs1057517972
Exac	rs1057517972
Gnomad	rs1057517972
Varsome	rs1057517972
LitVar	rs1057517972
Map	rs1057517972
PheGenI	rs1057517972
Biobank	rs1057517972
1000 genomes	rs1057517972
hgdp	rs1057517972
ensembl	rs1057517972
geneview	rs1057517972
scholar	rs1057517972
google	rs1057517972
pharmgkb	rs1057517972
gwascentral	rs1057517972
openSNP	rs1057517972
23andMe	rs1057517972
SNPshot	rs1057517972
SNPdbe	rs1057517972
MSV3d	rs1057517972
GWAS Ctlg	rs1057517972

Max Magnitude

0

ClinVar
Risk	rs1057517972(G;G)
Alt	rs1057517972(G;G)
Reference	Rs1057517972(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FAH
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.80445397A>G
CLNSRC
CLNACC	RCV000414667.1,