Variant (rsID / SNP)

rs10951942

rs10951942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C7ORF57, C7orf57. Location: chromosome 7, position 48,081,095. The table records no clinical significance for this variant.

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Reference-table entries

C7ORF57Not classified

Variant type: missense_variant
Chromosome / position: 7:48081095
HGVS: NM_001100159.3,c.220G>T,p.Ala74Ser
Allele change: Missense_A74S

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.