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1.

rs1374108 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    18:7669074 (GRCh38)
    18:7669072 (GRCh37)
    Canonical SPDI:
    NC_000018.10:7669073:G:A
    Gene:
    PTPRM (Varview)
    Functional Consequence:
    intron_variant,genic_upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.129345/11625 (ALFA)
    A=0.066667/6 (PRJEB36033)
    A=0.084665/53 (Chileans)
    A=0.096783/373 (ALSPAC)
    A=0.099515/369 (TWINSUK)
    A=0.1/60 (NorthernSweden)
    A=0.101852/22 (Qatari)
    A=0.11022/110 (GoNL)
    A=0.117317/24059 (GENOGRAPHIC)
    A=0.128748/146 (Daghestan)
    A=0.134821/604 (Estonian)
    A=0.15/6 (GENOME_DK)
    A=0.181001/1309 (Korea4K)
    A=0.181382/378 (HGDP_Stanford)
    A=0.183962/39 (Vietnamese)
    A=0.186689/547 (KOREAN)
    A=0.186814/27799 (GnomAD_genomes)
    A=0.189569/50177 (TOPMED)
    A=0.196658/15230 (TOMMO)
    A=0.21865/1095 (1000Genomes)
    A=0.224079/1435 (1000Genomes_30X)
    A=0.251057/475 (HapMap)
    G=0.367021/69 (SGDP_PRJ)
    G=0.5/7 (Siberian)
    HGVS:

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