rs121912685

Orientation

plus

Stabilized

plus

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

Make rs121912685(A;A)

Make rs121912685(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

73442356

Gene

AFP

is a	snp
is	mentioned by
dbSNP	rs121912685
dbSNP (classic)	rs121912685
ClinGen	rs121912685
ebi	rs121912685
HLI	rs121912685
Exac	rs121912685
Gnomad	rs121912685
Varsome	rs121912685
LitVar	rs121912685
Map	rs121912685
PheGenI	rs121912685
Biobank	rs121912685
1000 genomes	rs121912685
hgdp	rs121912685
ensembl	rs121912685
geneview	rs121912685
scholar	rs121912685
google	rs121912685
pharmgkb	rs121912685
gwascentral	rs121912685
openSNP	rs121912685
23andMe	rs121912685
SNPshot	rs121912685
SNPdbe	rs121912685
MSV3d	rs121912685
GWAS Ctlg	rs121912685

Max Magnitude

0

OMIM	104150
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121912685(A;A)
Alt	rs121912685(A;A)
Reference	Rs121912685(G;G)
Significance	Pathogenic
Disease	Alpha-fetoprotein deficiency
Variation	info
Gene	AFP
CLNDBN	Alpha-fetoprotein deficiency
Reversed	0
HGVS	NC_000004.11:g.74308073G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019800.29,