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NM_004626.3(WNT11):c.947G>A (p.Arg316His) AND Exstrophy-epispadias complex

Significance: Uncertain significance
ClinVar: RCV000172903

Variant: NM_004626.3(WNT11):c.947G>A (p.Arg316His)

Type: Variant
Allele: NM_004626.3(WNT11):c.947G>A (p.Arg316His) 187239
Gene:
Type: single nucleotide variant
Location: Chr11: 75898227 - assembly GRCh37
Chr11: 76187183 - assembly GRCh38
References: dbSNP: 758816226

Condition

Disease: Exstrophy-epispadias complex