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rs201249971

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201249971(A;T)
Make rs201249971(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position185519292
GeneLIPH
is asnp
is mentioned by
dbSNPrs201249971
dbSNP (classic)rs201249971
ClinGenrs201249971
ebirs201249971
HLIrs201249971
Exacrs201249971
Gnomadrs201249971
Varsomers201249971
LitVarrs201249971
Maprs201249971
PheGenIrs201249971
Biobankrs201249971
1000 genomesrs201249971
hgdprs201249971
ensemblrs201249971
geneviewrs201249971
scholarrs201249971
googlers201249971
pharmgkbrs201249971
gwascentralrs201249971
openSNPrs201249971
23andMers201249971
23andMe allrs201249971
SNPshotrs201249971
SNPdbers201249971
MSV3drs201249971
GWAS Ctlgrs201249971
Max Magnitude0
ClinVar
Risk rs201249971(T;T)
Alt rs201249971(T;T)
Reference Rs201249971(A;A)
Significance Probable-Pathogenic
Disease Hypotrichosis 7
Variation info
Gene LIPH
CLNDBN Hypotrichosis 7
Reversed 0
HGVS NC_000003.11:g.185237080A>T
CLNSRC
CLNACC RCV000490454.1,