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rs104895505

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104895505(A;A)
Make rs104895505(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
GeneNCR1, NLRP7
is asnp
is mentioned by
dbSNPrs104895505
ebirs104895505
HLIrs104895505
Exacrs104895505
Varsomers104895505
Maprs104895505
PheGenIrs104895505
hapmaprs104895505
1000 genomesrs104895505
hgdprs104895505
ensemblrs104895505
gopubmedrs104895505
geneviewrs104895505
scholarrs104895505
googlers104895505
pharmgkbrs104895505
gwascentralrs104895505
openSNPrs104895505
23andMers104895505
23andMe allrs104895505
SNP Nexus

SNPshotrs104895505
SNPdbers104895505
MSV3drs104895505
GWAS Ctlgrs104895505
Max Magnitude0
ClinVar
Risk rs104895505(A;A)
Alt rs104895505(A;A)
Reference rs104895505(G;G)
Significance Pathogenic
Disease Hydatidiform mole
Variation info
Gene NLRP7
CLNDBN Hydatidiform mole
Reversed 1
HGVS NC_000019.9:g.55445856C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001652.4,