Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A | Ancestral: C | Ambiguity code: M

Chromosome 3:41214354 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3198101

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2 sample genotypes.

Variant displays