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rs797044896

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044896(C;T)
Make rs797044896(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position53382595
GeneSMC1A
is asnp
is mentioned by
dbSNPrs797044896
ebirs797044896
HLIrs797044896
Exacrs797044896
Varsomers797044896
Maprs797044896
PheGenIrs797044896
hapmaprs797044896
1000 genomesrs797044896
hgdprs797044896
ensemblrs797044896
gopubmedrs797044896
geneviewrs797044896
scholarrs797044896
googlers797044896
pharmgkbrs797044896
gwascentralrs797044896
openSNPrs797044896
23andMers797044896
23andMe allrs797044896
SNP Nexus

SNPshotrs797044896
SNPdbers797044896
MSV3drs797044896
GWAS Ctlgrs797044896
Max Magnitude0
ClinVar
Risk rs797044896(T;T)
Alt rs797044896(T;T)
Reference rs797044896(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SMC1A
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.53409516G>A
CLNSRC
CLNACC RCV000190720.1,