rs387906751

Orientation

minus

Stabilized

minus

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

Make rs387906751(A;C)

Make rs387906751(C;C)

Reference

GRCh38 38.1/141

Chromosome

10

Position

4991861

Gene

AKR1C2

is a	snp
is	mentioned by
dbSNP	rs387906751
dbSNP (classic)	rs387906751
ClinGen	rs387906751
ebi	rs387906751
HLI	rs387906751
Exac	rs387906751
Gnomad	rs387906751
Varsome	rs387906751
LitVar	rs387906751
Map	rs387906751
PheGenI	rs387906751
Biobank	rs387906751
1000 genomes	rs387906751
hgdp	rs387906751
ensembl	rs387906751
geneview	rs387906751
scholar	rs387906751
google	rs387906751
pharmgkb	rs387906751
gwascentral	rs387906751
openSNP	rs387906751
23andMe	rs387906751
SNPshot	rs387906751
SNPdbe	rs387906751
MSV3d	rs387906751
GWAS Ctlg	rs387906751

Max Magnitude

0

ClinVar
Risk	rs387906751(C;C)
Alt	rs387906751(C;C)
Reference	Rs387906751(A;A)
Significance	Pathogenic
Disease	46
Variation	info
Gene	AKR1C2
CLNDBN	46,XY sex reversal 8
Reversed	1
HGVS	NC_000010.10:g.5034053T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022969.3,