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rs201835496

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201835496(C;G)
Make rs201835496(G;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position5302662
GenePROKR2
is asnp
is mentioned by
dbSNPrs201835496
ebirs201835496
HLIrs201835496
Exacrs201835496
Varsomers201835496
Maprs201835496
PheGenIrs201835496
hapmaprs201835496
1000 genomesrs201835496
hgdprs201835496
ensemblrs201835496
gopubmedrs201835496
geneviewrs201835496
scholarrs201835496
googlers201835496
pharmgkbrs201835496
gwascentralrs201835496
openSNPrs201835496
23andMers201835496
23andMe allrs201835496
SNP Nexus

SNPshotrs201835496
SNPdbers201835496
MSV3drs201835496
GWAS Ctlgrs201835496
Max Magnitude0
ClinVar
Risk rs201835496(G;G)
Alt rs201835496(G;G)
Reference rs201835496(C;C)
Significance Pathogenic
Disease Kallmann syndrome 3
Variation info
Gene PROKR2
CLNDBN Kallmann syndrome 3
Reversed 0
HGVS NC_000020.10:g.5283308C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144714.3,