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rs752673677

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs752673677(A;A)
Make rs752673677(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position24338044
GeneGRHL3
is asnp
is mentioned by
dbSNPrs752673677
ebirs752673677
HLIrs752673677
Exacrs752673677
Varsomers752673677
Maprs752673677
PheGenIrs752673677
hapmaprs752673677
1000 genomesrs752673677
hgdprs752673677
ensemblrs752673677
gopubmedrs752673677
geneviewrs752673677
scholarrs752673677
googlers752673677
pharmgkbrs752673677
gwascentralrs752673677
openSNPrs752673677
23andMers752673677
23andMe allrs752673677
SNP Nexus

SNPshotrs752673677
SNPdbers752673677
MSV3drs752673677
GWAS Ctlgrs752673677
Max Magnitude0
ClinVar
Risk rs752673677(A;A)
Alt rs752673677(A;A)
Reference rs752673677(G;G)
Significance Pathogenic
Disease Van der Woude syndrome 2
Variation info
Gene GRHL3
CLNDBN Van der Woude syndrome 2
Reversed 0
HGVS NC_000001.10:g.24664534G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087751.3,