Variant (rsID / SNP)

rs11736872

rs11736872 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR17. Location: chromosome 4, position 177,100,644. The table records no clinical significance for this variant.

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Reference-table entries

WDR17Not classified

Variant type: missense_variant
Chromosome / position: 4:177100644
HGVS: NM_170710.5,c.3883G>A,p.Ala1295Thr
Allele change: Missense_A1287T

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.