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Variant (rsID / SNP)

rs11071896

ZWILCH

rs11071896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZWILCH. Location: chromosome 15, position 66,821,250. The table records no clinical significance for this variant.

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Reference-table entries

ZWILCHNot classified
Variant type
missense_variant
Chromosome / position
15:66821250
HGVS
NM_017975.5,c.1030A>G,p.Ser344Gly
Allele change
Missense_S230G

Public references

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