Variant (rsID / SNP)

rs12507775

rs12507775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RASSF6. Location: chromosome 4, position 74,451,073. The table records no clinical significance for this variant.

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Reference-table entries

RASSF6Not classified

Variant type: missense_variant
Chromosome / position: 4:74451073
HGVS: NM_201431.2,c.487T>C,p.Ser163Pro
Allele change: Missense_S131P

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.