rs1060505055

Orientation

plus

Stabilized

plus

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

Make rs1060505055(G;T)

Make rs1060505055(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

31759476

Gene	MSH5, MSH5-SAPCD1

is a	snp
is	mentioned by
dbSNP	rs1060505055
dbSNP (classic)	rs1060505055
ClinGen	rs1060505055
ebi	rs1060505055
HLI	rs1060505055
Exac	rs1060505055
Gnomad	rs1060505055
Varsome	rs1060505055
LitVar	rs1060505055
Map	rs1060505055
PheGenI	rs1060505055
Biobank	rs1060505055
1000 genomes	rs1060505055
hgdp	rs1060505055
ensembl	rs1060505055
geneview	rs1060505055
scholar	rs1060505055
google	rs1060505055
pharmgkb	rs1060505055
gwascentral	rs1060505055
openSNP	rs1060505055
23andMe	rs1060505055
SNPshot	rs1060505055
SNPdbe	rs1060505055
MSV3d	rs1060505055
GWAS Ctlg	rs1060505055

Max Magnitude

0

ClinVar
Risk	rs1060505055(T;T)
Alt	rs1060505055(T;T)
Reference	Rs1060505055(G;G)
Significance	Pathogenic
Disease	Premature ovarian failure 13
Variation	info
Gene	MSH5-SAPCD1 MSH5
CLNDBN	Premature ovarian failure 13
Reversed	0
HGVS	NC_000006.11:g.31727253G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000477966.1,