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Variant (rsID / SNP)

rs4951168

TMEM81

rs4951168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM81. Location: chromosome 1, position 205,053,219. The table records no clinical significance for this variant.

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Reference-table entries

TMEM81Not classified
Variant type
missense_variant
Chromosome / position
1:205053219
HGVS
NM_203376.2,c.230G>A,p.Arg77Gln
Allele change
Missense_R77Q

Public references

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