Variant (rsID / SNP)

rs9649951

rs9649951 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZHX2. Location: chromosome 8, position 123,964,819. The table records no clinical significance for this variant.

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Reference-table entries

ZHX2Not classified

Variant type: missense_variant
Chromosome / position: 8:123964819
HGVS: NM_001362797.2,c.1069G>A,p.Val357Met
Allele change: Missense_V357M

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.