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rs104895504

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104895504(A;A)
Make rs104895504(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
GeneNLRP7
is asnp
is mentioned by
dbSNPrs104895504
ebirs104895504
HLIrs104895504
Exacrs104895504
Varsomers104895504
Maprs104895504
PheGenIrs104895504
hapmaprs104895504
1000 genomesrs104895504
hgdprs104895504
ensemblrs104895504
gopubmedrs104895504
geneviewrs104895504
scholarrs104895504
googlers104895504
pharmgkbrs104895504
gwascentralrs104895504
openSNPrs104895504
23andMers104895504
23andMe allrs104895504
SNP Nexus

SNPshotrs104895504
SNPdbers104895504
MSV3drs104895504
GWAS Ctlgrs104895504
Max Magnitude0
ClinVar
Risk rs104895504(A;A)
Alt rs104895504(A;A)
Reference rs104895504(G;G)
Significance Pathogenic
Disease Hydatidiform mole
Variation info
Gene NLRP7
CLNDBN Hydatidiform mole
Reversed 1
HGVS NC_000019.9:g.55452298C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001651.3,