rs104893667

Orientation

minus

Stabilized

minus

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

Make rs104893667(C;G)

Make rs104893667(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

31580823

Gene

SRD5A2

is a	snp
is	mentioned by
dbSNP	rs104893667
dbSNP (classic)	rs104893667
ClinGen	rs104893667
ebi	rs104893667
HLI	rs104893667
Exac	rs104893667
Gnomad	rs104893667
Varsome	rs104893667
LitVar	rs104893667
Map	rs104893667
PheGenI	rs104893667
Biobank	rs104893667
1000 genomes	rs104893667
hgdp	rs104893667
ensembl	rs104893667
geneview	rs104893667
scholar	rs104893667
google	rs104893667
pharmgkb	rs104893667
gwascentral	rs104893667
openSNP	rs104893667
23andMe	rs104893667
SNPshot	rs104893667
SNPdbe	rs104893667
MSV3d	rs104893667
GWAS Ctlg	rs104893667

Max Magnitude

0

OMIM	607306
Desc
Variant	0015
Related	also

ClinVar
Risk	rs104893667(G;G) rs104893667(T;T)
Alt	rs104893667(G;G) rs104893667(T;T)
Reference	Rs104893667(C;C)
Significance	Pathogenic
Disease	Micropenis
Variation	info
Gene	SRD5A2
CLNDBN	Micropenis
Reversed	1
HGVS	NC_000002.11:g.31805892G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003514.5,