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Variant (rsID / SNP)

rs34955597

EFCAB6

rs34955597 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFCAB6. Location: chromosome 22, position 43,950,853. The table records no clinical significance for this variant.

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Reference-table entries

EFCAB6Not classified
Variant type
missense_variant
Chromosome / position
22:43950853
HGVS
NM_022785.4,c.3544A>C,p.Thr1182Pro
Allele change
Missense_T1030P

Public references

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